The Best Chemistry compound:2-Aminobenzamide

HPLC of Formula: C7H8N2O. Welcome to talk about 88-68-6, If you have any questions, you can contact Xie, ZB; Lan, J; Yan, LY; Chen, XH; Li, Q; Meng, J; Le, ZG or send Email.

Recently I am researching about MOLECULAR-OXYGEN; EFFICIENT; 2,3-DIHYDROQUINAZOLIN-4(1H)-ONES; OXIDATION; ALKENES; DERIVATIVES; DESIGN; FACILE; CYCLIZATION; OZONOLYSIS, Saw an article supported by the National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [11765002, 21966003]; Science and Technology Project of Jiangxi [20192BBH80012]. HPLC of Formula: C7H8N2O. Published in ROYAL SOC CHEMISTRY in CAMBRIDGE ,Authors: Xie, ZB; Lan, J; Yan, LY; Chen, XH; Li, Q; Meng, J; Le, ZG. The CAS is 88-68-6. Through research, I have a further understanding and discovery of 2-Aminobenzamide

This is the first report on a facile tandem route for synthesizing quinazolinones at room temperature from various aminobenzamides and in situ-generated aldehydes. The latter was formed via C=C bond cleavage, and the overall reaction proceeded using molecular oxygen as a clean oxidant in the absence of a photocatalyst. Visible light, which was indispensable for the entire course of the reaction, played multiple roles. It initially cleaved styrene to an aldehyde, then facilitated its cyclization with an o-substituted aniline, and finally promoted the dehydrogenation of the cyclized intermediate. The previous step provided the feedstock for the next step in the reaction, thereby preventing volatilization, oxidation, and polymerization of the aldehyde. Thus, the overall process is simple, environmentally benign, and economically feasible.

HPLC of Formula: C7H8N2O. Welcome to talk about 88-68-6, If you have any questions, you can contact Xie, ZB; Lan, J; Yan, LY; Chen, XH; Li, Q; Meng, J; Le, ZG or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

What Kind of Chemistry Facts Are We Going to Learn About C7H8N2O

Welcome to talk about 88-68-6, If you have any questions, you can contact Eberl, HC; Werner, T; Reinhard, FB; Lehmann, S; Thomson, D; Chen, PL; Zhang, CY; Rau, C; Muelbaier, M; Drewes, G; Drewry, D; Bantscheff, M or send Email.. Quality Control of 2-Aminobenzamide

An article Chemical proteomics reveals target selectivity of clinical Jak inhibitors in human primary cells WOS:000488481500022 published article about CYCLIN-DEPENDENT KINASE; DRUG TARGET; OFF-TARGET; KINOME; MUTATION; IDENTIFICATION; TOFACITINIB; RUXOLITINIB; DISCOVERY; PLACEBO in [Eberl, H. Christian; Werner, Thilo; Reinhard, Friedrich B.; Lehmann, Stephanie; Thomson, Douglas; Rau, Christina; Muelbaier, Marcel; Drewes, Gerard; Bantscheff, Marcus] Cellzome GmbH, Meyerhofstr 1, D-69117 Heidelberg, Germany; [Chen, Peiling; Zhang, Cunyu] GlaxoSmithKline, 709 Swedeland Rd 1539, King Of Prussia, PA 19406 USA; [Drewry, David] GlaxoSmithKline, 5 Moore Dr, Res Triangle Pk, NC 27709 USA; [Drewry, David] Univ North Carolina Chapel Hill, UNC Eshelman Sch Pharm, Struct Genom Consortium, 120 Mason Farm Rd, Chapel Hill, NC 27599 USA in 2019, Cited 60. Quality Control of 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Kinobeads are a set of promiscuous kinase inhibitors immobilized on sepharose beads for the comprehensive enrichment of endogenously expressed protein kinases from cell lines and tissues. These beads enable chemoproteomics profiling of kinase inhibitors of interest in dose-dependent competition studies in combination with quantitative mass spectrometry. We present improved bead matrices that capture more than 350 protein kinases and 15 lipid kinases from human cell lysates, respectively. A multiplexing strategy is suggested that enables determination of apparent dissociation constants in a single mass spectrometry experiment. Miniaturization of the procedure enabled determining the target selectivity of the clinical BCR-ABL inhibitor dasatinib in peripheral blood mononuclear cell (PBMC) lysates from individual donors. Profiling of a set of Jak kinase inhibitors revealed kinase off-targets from nearly all kinase families underpinning the need to profile kinase inhibitors against the kinome. Potently bound off-targets of clinical inhibitors suggest polypharmacology, e.g. through MRCK alpha and beta, which bind to decernotinib with nanomolar affinity.

Welcome to talk about 88-68-6, If you have any questions, you can contact Eberl, HC; Werner, T; Reinhard, FB; Lehmann, S; Thomson, D; Chen, PL; Zhang, CY; Rau, C; Muelbaier, M; Drewes, G; Drewry, D; Bantscheff, M or send Email.. Quality Control of 2-Aminobenzamide

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

New learning discoveries about C7H8N2O

Computed Properties of C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Krapf, MK; Gallus, J; Spindler, A; Wiese, M or concate me.

Computed Properties of C7H8N2O. In 2019 EUR J MED CHEM published article about RESISTANCE PROTEIN BCRP/ABCG2; MULTIDRUG-RESISTANCE; SELECTIVE INHIBITORS; DRUG-RESISTANCE; HIGHLY POTENT; CANCER; TRANSPORTER; BCRP; EXPRESSION; CELLS in [Krapf, Michael K.; Gallus, Jennifer; Spindler, Anna; Wiese, Michael] Univ Bonn, Inst Pharmaceut, Immenburg 4, D-53121 Bonn, Germany in 2019, Cited 51. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6.

Multidrug resistance (MDR) is a major obstacle for effective chemotherapeutic treatment of cancer frequently leading to failure of the therapy. MDR is often associated with the overexpression of ABC transport proteins like ABCB1 or ABCG2 which efflux harmful substances out of cells at the cost of ATP hydrolysis. One way to overcome MDR is to apply potent inhibitors of ABC transporters to restore the sensitivity of the cells toward cytostatic agents. This study focusses on the synthesis and evaluation of novel 2,4-disubstituted quinazoline derivatives regarding the structure-activity-relationship (SAR), their ability to reverse MDR and their mode of interaction with ABCG2. Hence, the inhibitory potency and selectivity toward ABCG2 was determined. Moreover, the intrinsic cytotoxicity and the reversal of MDR were investigated. Interaction type studies with the substrate Hoechst 33342 and conformational analyses of ABCG2 with 5D3 monoclonal antibody were performed for a better understanding of the underlying mechanisms. In our study we could further enhance the inhibitory effect against ABCG2 (compound 31, IC50: 55 nM) and identify the structural features that are crucial for inhibitory potency, the impact on transport activity and binding to the protein. (C) 2018 Elsevier Masson SAS. All rights reserved,

Computed Properties of C7H8N2O. About 2-Aminobenzamide, If you have any questions, you can contact Krapf, MK; Gallus, J; Spindler, A; Wiese, M or concate me.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Awesome and Easy Science Experiments about 64-10-8

COA of Formula: C7H8N2O. Welcome to talk about 64-10-8, If you have any questions, you can contact Sakakibara, K; Moriki, Y; Tsujn, Y or send Email.

Recently I am researching about MICROFIBRILLATED CELLULOSE; POLYMER NANOCOMPOSITES; ELASTIC-MODULUS; MECHANICAL-PROPERTIES; CRYSTALLINE REGIONS; SURFACE; GREEN; DISSOLUTION; BIOCOMPOSITES; NANOCELLULOSE, Saw an article supported by the National Agriculture and Food Research Organization (NARO) Bio-oriented Technology Research Advancement Institution; JSPS KAKENHIMinistry of Education, Culture, Sports, Science and Technology, Japan (MEXT)Japan Society for the Promotion of ScienceGrants-in-Aid for Scientific Research (KAKENHI) [17H06238]; DIC Corporation; Daio Paper Corporation. COA of Formula: C7H8N2O. Published in AMER CHEMICAL SOC in WASHINGTON ,Authors: Sakakibara, K; Moriki, Y; Tsujn, Y. The CAS is 64-10-8. Through research, I have a further understanding and discovery of 1-Phenylurea

Production of nanocomposites from macro-scale materials in situ in a melting compounder is highly desirable yet challenging. In this study, we develop a highly efficient approach for the preparation of cellulose nanofiber (CNF)-reinforced high-density polyethylene (HDPE) composite materials from as-received wood pulp fibers, in which nanofibrillation-assisting plasticizers (urea and urea derivatives) and a diblock copolymer dispersant are used. The most effective plasticizer is urea, which plays a crucial role in producing CNF with less fragmentation during the kneading step, owing to the plasticization/nanofibrillation and the reaction with hydroxyl groups of cellulose fibers into a carbamate. The diblock copolymer as a dispersant enables the stabilization of the appropriate dispersion of the produced CNF in nonpolar HDPE. The resulting composites exhibit significantly improved mechanical properties, including a 6.9-fold increase in the Youngs modulus with 10 wt % loading of wood pulp fibers over that of neat HDPE.

COA of Formula: C7H8N2O. Welcome to talk about 64-10-8, If you have any questions, you can contact Sakakibara, K; Moriki, Y; Tsujn, Y or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Why Are Children Getting Addicted To 3-Nitrobenzaldehyde

COA of Formula: C7H5NO3. Bye, fridends, I hope you can learn more about C7H5NO3, If you have any questions, you can browse other blog as well. See you lster.

In 2021.0 APPL CATAL A-GEN published article about HETEROGENEOUS CATALYST; EFFICIENT; INHIBITORS; DESIGN; OXIDE; DERIVATIVES; RECEPTOR; GYRASE in [Yadav, Priyanka; Kakati, Praachi; Singh, Preeti; Awasthi, Satish K.] Univ Delhi, Dept Chem, Chem Biol Lab, Delhi 110007, India in 2021.0, Cited 39.0. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6. COA of Formula: C7H5NO3

This work represents the design and synthesis of efficient sulfonated cobalt ferrite solid acid catalyst. The synthesized solid acid green catalyst was characterized using various techniques viz. FT-IR, powder XRD, SEM, TEM and VSM. The obtained catalyst was used to synthesize biologically significant 2-substituted benzimidazole derivatives by condensation between o-phenylenediamine with various aromatic, aliphatic and heterocyclic aldehydes. High yield (up to 98 %), short reaction time (10-25 min), mild reaction condition, wide functional group tolerance, easy work-up procedure and excellent values of green chemistry metrices such as lower E factor (0.126), high RME value (88.83 %), carbon efficiency (100 %) and high atom economy (AE) value (90.65 %), are some salient features of the present catalytic system. Moreover, the catalyst recovery by simply using an external magnet and catalyst reusability up to 7 times without any significant loss in catalytic efficiency are some additional remarkable features of the current protocol.

COA of Formula: C7H5NO3. Bye, fridends, I hope you can learn more about C7H5NO3, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Chemistry Milestones Of 2-Aminobenzamide

Recommanded Product: 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Xie, ZB; Li, HX; Liu, LS; Lan, J; Hu, ZY; Le, ZG or send Email.

Authors Xie, ZB; Li, HX; Liu, LS; Lan, J; Hu, ZY; Le, ZG in SCIENCE PRESS published article about ONE-POT SYNTHESIS; ENZYME; 2,3-DIHYDROQUINAZOLIN-4(1H)-ONES; EFFICIENT; NANOCATALYST; PROMISCUITY; ACYLASE; MILD in [Xie, Zongbo; Li, Hongxia; Liu, Liansheng; Lan, Jin; Hu, Zhiyu; Le, Zhanggao] East China Univ Technol, Dept Appl Chem, Nanchang 330013, Jiangxi, Peoples R China in 2019, Cited 41. Recommanded Product: 2-Aminobenzamide. The Name is 2-Aminobenzamide. Through research, I have a further understanding and discovery of 88-68-6

Alkaline protease-catalyzed synthesis of quinazolinone derivatives was developed between beta-keotester and o-aminobenzamide. Because ethanol is one kind of eco-friendly solvents, this method can reduce the impact of solvents on the environment. Alkaline protease as a biocatalyst has many advantages, e.g. high catalytic activity, environmentally friendly, wide variety of sources and simple operation. In addition, a variety of quinazolinone derivatives was obtained with good to excellent yields just using 2000 U alkaline protease as catalyst.

Recommanded Product: 2-Aminobenzamide. Welcome to talk about 88-68-6, If you have any questions, you can contact Xie, ZB; Li, HX; Liu, LS; Lan, J; Hu, ZY; Le, ZG or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Search for chemical structures by a sketch :C7H8N2O

Quality Control of 1-Phenylurea. Welcome to talk about 64-10-8, If you have any questions, you can contact Grossi, F; Genova, C; Crino, L; Delmonte, A; Turci, D; Signorelli, D; Passaro, A; Parra, HS; Catino, A; Landi, L; Gelsomino, F; Tiseo, M; Puppo, G; Roila, F; Ricciardi, S; Tonini, G; Cognetti, F; Toschi, L; Tassinari, D; Scoppola, A; Giannarelli, D; Cortesi, E or send Email.

I found the field of Oncology very interesting. Saw the article Real-life results from the overall population and key subgroups within the Italian cohort of nivolumab expanded access program in non-squamous non-small cell lung cancer published in 2019.0. Quality Control of 1-Phenylurea, Reprint Addresses Grossi, F (corresponding author), Fdn IRCCS Ca Granda Osped Maggiore Policlin, Med Oncol Unit, Milan, Italy.. The CAS is 64-10-8. Through research, I have a further understanding and discovery of 1-Phenylurea

Background: Nivolumab was the first immune checkpoint inhibitor approved for previously treated advanced nonesmall cell lung cancer (NSCLC). Before its introduction in the market, nivolumab was made available to NSCLC patients through an expanded access program (EAP). Here we present the Italian cohort of patients with non-squamous NSCLC enrolled in a worldwide nivolumab EAP, with subgroup analyses involving elderly patients, patients with central nervous system (CNS) metastases and patients receiving nivolumab beyond progression. Methods: Pretreated patients with advanced non-squamous NSCLC received nivolumab at 3 mg/kg every 2 weeks up to 24 months. Efficacy data (investigator-assessed tumour response, progression date and survival) and safety data were collected. Findings: 1588 patients were treated across 153 Italian centres. Overall response rate and disease control rate were 18% and 44%, respectively; median overall survival (OS) was 11.3 months (95% CI: 10.2-12.4). Elderly patients (>= 70 n = 522; >= 75 n = 232) achieved outcomes similar to the global study population; patients with CNS metastases (n = 409) had an OS of 8.6 months (95% CI: 6.4-10.8), and a 1-year OS rate of 43%. Nivolumab was administered beyond progression to 276 patients (26%), 57 of whom achieved subsequent disease control; the median OS of patients receiving nivolumab beyond progression was 16.2 months (95% CI: 14.0-18.4), while 1-year OS rate was 62%. Interpretation: To date, this is the largest clinical experience with nivolumab in a real-world setting. Our data support its use in clinical practice for pretreated non-squamous NSCLC, including patients with older age or CNS metastases. (C) 2019 Elsevier Ltd. All rights reserved.

Quality Control of 1-Phenylurea. Welcome to talk about 64-10-8, If you have any questions, you can contact Grossi, F; Genova, C; Crino, L; Delmonte, A; Turci, D; Signorelli, D; Passaro, A; Parra, HS; Catino, A; Landi, L; Gelsomino, F; Tiseo, M; Puppo, G; Roila, F; Ricciardi, S; Tonini, G; Cognetti, F; Toschi, L; Tassinari, D; Scoppola, A; Giannarelli, D; Cortesi, E or send Email.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

Chemical Properties and Facts of C7H5NO3

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Zhou, SY; Guan, JY; Li, ZQ; Zhang, QF; Zheng, JF; Li, SH; Zhang, SB or concate me.. Formula: C7H5NO3

Zhou, SY; Guan, JY; Li, ZQ; Zhang, QF; Zheng, JF; Li, SH; Zhang, SB in [Zhou, Shengyang; Guan, Jiayu; Li, Ziqin; Zhang, Qifeng; Zheng, Jifu; Li, Shenghai; Zhang, Suobo] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Ecomat, Changchun 130022, Peoples R China; [Zhou, Shengyang; Guan, Jiayu; Li, Ziqin; Li, Shenghai; Zhang, Suobo] Univ Sci & Technol China, Hefei 230026, Peoples R China published Synthesis of Fluorinated Poly(phenyl-alkane)s of Intrinsic Microporosity by Regioselective Aldehyde (A(2)) + Aromatics (B-2) Friedel-Crafts Polycondensation in 2021.0, Cited 45.0. Formula: C7H5NO3. The Name is 3-Nitrobenzaldehyde. Through research, I have a further understanding and discovery of 99-61-6.

The design of functionalized porous materials is an important research direction in material science, especially for fluorine-containing materials with enhanced thermal/oxidative stability, lower dielectric constants, and better gas-selective permeation. In this work, a series of poly(phenyl-alkane)s of intrinsic microporosity (PIM-xR) were synthesized by the methanesulfonic acid-catalyzed Friedel-Crafts hydroxyalkylation polycondensation of contorted and rigid multibenzene and benzaldehyde derivatives. The PIM-xR exhibited good thermal stability, excellent solution processability, and high Brunauer-Emmett-Teller (BET) surface areas (400-1200 m(2) g(-1)). The physicochemical properties and applications of PIM-xR could be tuned by the type, quantity, distribution, and postmodification of substituents on the benzaldehyde derivatives. Unlike other contorted and rigid multibenzene derivatives, only electron-rich spirobiindane derivatives directly produced soluble, linear, high-molecular-weight polymers without cross-linking because spirobiindane possesses three t-butyl-like structural units that provide large steric hindrance at potential reactive sites. Subsequently, a series of fluorinated PIMs (PIM-xF) with different fluorine contents and distributions were explored, and the relationship between the microporosity of PIM-xR and degrees of rotational freedom of the polymer chains was analyzed using these PIM-xF. Flexible and transparent PIM-xF membranes were easily obtained by solution processing and exhibited high gas permeabilities and moderate permeability selectivity. In particular, the CO2/N-2 separation performance of the PIM-5F membrane exceeded the 2008 Robeson’s upper bound (P-CO2 = 3240 barrer and alpha((CO2/N2)) = 27.9). This work provides a facile method for the precise design and preparation of fluorinated or other functionalized porous materials for environmental and energy applications.

About 3-Nitrobenzaldehyde, If you have any questions, you can contact Zhou, SY; Guan, JY; Li, ZQ; Zhang, QF; Zheng, JF; Li, SH; Zhang, SB or concate me.. Formula: C7H5NO3

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

What unique challenges do researchers face in 90-44-8

Formula: C14H10O. Bye, fridends, I hope you can learn more about C14H10O, If you have any questions, you can browse other blog as well. See you lster.

An article Insight into the chemoselective aromatic vs. side-chain hydroxylation of alkylaromatics with H2O2 catalyzed by a non-heme imine-based iron complex WOS:000609012400013 published article about HYDROGEN-PEROXIDE; C-H; POLYAZADENTATE COMPLEXES; SELECTIVE HYDROXYLATION; IRON(IV)-OXO COMPLEXES; EFFICIENT CATALYSTS; BENZOIC-ACIDS; OXIDATION; BENZENE; PHENOL in [Ticconi, Barbara; Capocasa, Giorgio; Cerrato, Andrea; Di Stefano, Stefano; Lapi, Andrea; Marincioni, Beatrice; Lanzalunga, Osvaldo] Univ Roma La Sapienza, Dipartimento Chim, Ple A Moro 5, I-00185 Rome, Italy; [Ticconi, Barbara; Capocasa, Giorgio; Cerrato, Andrea; Di Stefano, Stefano; Lapi, Andrea; Marincioni, Beatrice; Lanzalunga, Osvaldo] Univ Roma La Sapienza, Dipartimento Chim, Sez Meccanismi Reaz, Ist CNR & Sistemi Biol ISB CNR, Ple A Moro 5, I-00185 Rome, Italy; [Olivo, Giorgio] Univ Girona, Inst Quim Computac & Catalisi IQCC, Campus Montilivi,C Maria Aurelia Capmany 69, Girona 17003, Spain; [Olivo, Giorgio] Univ Girona, Dept Quim, Campus Montilivi,C Maria Aurelia Capmany 69, Girona 17003, Spain; [Olivo, Giorgio] Univ Girona, Inst Quim Computac & Catalisi IQCC, Campus Montilivi, Girona 17071, Spain; [Olivo, Giorgio] Univ Girona, Dept Quim, Campus Montilivi, Girona 17071, Spain in 2021, Cited 75. Formula: C14H10O. The Name is Anthrone. Through research, I have a further understanding and discovery of 90-44-8

The oxidation of a series of alkylaromatic compounds with H2O2 catalyzed by an imine-based non-heme iron complex prepared in situ by reaction of 2-picolylaldehyde, 2-picolylamine, and Fe(OTf)(2) in a 2 : 2 : 1 ratio leads to a marked chemoselectivity for aromatic ring hydroxylation over side-chain oxidation. This selectivity is herein investigated in detail. Side-chain/ring oxygenated product ratio was found to increase upon decreasing the bond dissociation energy (BDE) of the benzylic C-H bond in line with expectation. Evidence for competitive reactions leading either to aromatic hydroxylation via electrophilic aromatic substitution or side-chain oxidation via benzylic hydrogen atom abstraction, promoted by a metal-based oxidant, has been provided by kinetic isotope effect analysis.

Formula: C14H10O. Bye, fridends, I hope you can learn more about C14H10O, If you have any questions, you can browse other blog as well. See you lster.

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

The Shocking Revelation of 90-44-8

Welcome to talk about 90-44-8, If you have any questions, you can contact Kuang, L; Zhong, M; Sang, XY; Huang, ZZ or send Email.. Product Details of 90-44-8

I found the field of Polymer Science very interesting. Saw the article Synthesis and characterization of novel polyimides based on 10,10-bis[4-(4-aminophenoxy)-3-methylphenyl]-9(10H)-anthrone published in 2020. Product Details of 90-44-8, Reprint Addresses Zhong, M; Huang, ZZ (corresponding author), Jiangxi Normal Univ, Key Lab Funct Small Organ Mol, Minist Educ, Nanchang 330022, Jiangxi, Peoples R China.. The CAS is 90-44-8. Through research, I have a further understanding and discovery of Anthrone

10,10-Bis[4-(4-aminophenoxy)-3-methylphenyl]-9(10H)-anthrone, as a novel aromatic diamine, was synthesized from anthrone by three-step process. A series of polyimides containing methyl substituents and 9(10H)-anthrone pendant groups was prepared from this diamine with various aromatic dianhydridesviathe poly(amic acid) (PAA) precursors and subsequent thermal or chemical imidization procedure. Inherent viscosities of PAAs are between 0.87 and 1.58 dL/g, and the corresponding polyimides have the weight-average molecular weight and number-average molecular weight in the range of 49,400-64,200 and 28,700-37,700, respectively. Most of the polyimides obtained through the chemical cyclodehydration method are soluble in NMP, DMF, DMAc, Py andm-cresol at room temperature. These polyimides have glass transition temperatures of 289-313 degrees C, 10% weight loss temperatures of 484-524 degrees C, char yields of 55-63% at 800 degrees C, and temperature at the maximum-rate degradation of 560-584 degrees C in nitrogen, respectively. The polyimide films obtained through the thermal imidization have tensile strength of 76.43-119.74 MPa, elongation at break of 6.93-12.33%, and tensile modulus of 1.91-2.38 GPa.

Welcome to talk about 90-44-8, If you have any questions, you can contact Kuang, L; Zhong, M; Sang, XY; Huang, ZZ or send Email.. Product Details of 90-44-8

Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem