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Substituted anilines and vinyl sulfone undergo a facile double Michael addition to form substituted phenylthiomorpholine dioxide, catalyzed with AlCl3 or H3PO4. Scope and conditions were explored. (C) 2003 Elsevier Science Ltd. All rights reserved.

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

 

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In chemical reaction engineering, simulations are useful for investigating and optimizing a particular reaction process or system. In an article, author is Martynov, Alexander V., once mentioned the application of 90-01-7, Name is Salicyl Alcohol, molecular formula is C7H8O2, molecular weight is 124.1372, MDL number is MFCD00004617, category is thiomorpholine. Now introduce a scientific discovery about this category, Formula: https://www.ambeed.com/products/90-01-7.html.

An efficient method for preparation of earlier unknown S-oxide of 2(E),6(E)-bis(chloromethylidene)-4-thiomorpholinamine by oxidation of 2(E), 6(E)-bis(chloromethylidene)-4-thiomorpholinamine hydrochloride with hydrogen peroxide in H2O or EtOH/H2O followed by the reaction mixture neutralization with Na2CO3 has been described. Interaction of the S-oxide with acetaldehyde, butanal, benzaldehyde, 4-methoxybenzaldehyde and 4-pyridinecarboxaldehyde in EtOH, C6H6, in the mixture of acetonitrile and ethanol or ethanol and benzene affords the unknown hydrazones, N-organylmethylidene-2(E), 6(E)-bis(chloromethylidene)-4-thiomorpholinamine-1-oxides. [GRAPHICS] .

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

 

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When developing chemical systems it’s of course important to gain a deep understanding of the chemical reaction process. In an article, author is Medcalf, BD, once mentioned the application of 90-01-7, Name is Salicyl Alcohol, molecular formula is C7H8O2, molecular weight is 124.1372, MDL number is MFCD00004617, category is thiomorpholine. Now introduce a scientific discovery about this category, Application of 90-01-7.

The behavior of a non-incinerative reductive thermal cocurrent flow gasification process (ChemChar Process) when used to treat representative sulfur compounds is reported. Gasification of 1,3-benzenedisulfonic acid, thiomorpholine, and sulfuric acid converts the sulfur in these compounds to H2S, OCS, and elemental sulfur. The H2S and OCS are released in the synthesis with the gas product from which they can be scrubbed, with the elemental sulfur being deposited on the char matrix. No production of sulfur dioxide was detected. Gasified sulfur products recovered amounted to 89-114% of the total sulfur present in the sulfur compounds gasified, although exact mass balances could not be obtained due to the sulfur present in the char. (C) 1998 Elsevier Science Ltd. All rights reserved.

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

 

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Reference of 90-01-7, Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more.90-01-7, Name is Salicyl Alcohol, SMILES is C1=CC=CC(=C1O)CO, belongs to thiomorpholine compound. In a article, author is Mancy, Ahmed, introduce new discover of the category.

Bacterial resistance to antibiotics is presently one of the most pressing healthcare challenges and necessitates the discovery of new antibacterials with unique chemical scaffolds. However, the determination of the optimal balance between structural requirements for pharmacological action and pharmacokinetic properties of novel antibacterial compounds is a significant challenge in drug development. The incorporation of lipophilic moieties within a compound’s core structure can enhance biological activity but have a deleterious effect on drug-like properties. In this Article, the lipophilicity of alkynylphenylthiazoles, previously identified as novel antibacterial agents, was reduced by introducing cyclic amines to the lipophilic side chain. In this regard, substitution with methylpiperidine (compounds 14-16) and thiomorpholine (compound 19) substituents significantly enhanced the aqueous solubility profile of the new compounds more than 150-fold compared to the first-generation lead compound 1b. Consequently, the pharmacokinetic profile of compound 15 was significantly enhanced with a notable improvement in both half-life and the time the compound’s plasma concentration remained above its minimum inhibitory concentration (MIC) against methicillin-resistant Staphylococcus aureus (MRSA). In addition, compounds 14-16 and 19 were found to exert a bactericidal mode of action against MRSA and were not susceptible to resistance formation after 14 serial passages. Moreover, these compounds (at 2X MIC) were superior to the antibiotic vancomycin in the disruption of the mature MRSA biofilm. The modifications to the alkynylphenylthiazoles reported herein successfully improved the pharmacokinetic profile of this new series while maintaining the compounds’ biological activity against MRSA.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

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Product Details of 90-01-7, Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more.90-01-7, Name is Salicyl Alcohol, SMILES is C1=CC=CC(=C1O)CO, belongs to thiomorpholine compound. In a article, author is Yan, Shanshan, introduce new discover of the category.

A series of novel oxazolidinone antibiotics having [2.2.1] and [2.2.2] bicyclic oxazine moieties at the C-5 side chain of the A-ring was synthesized by nitroso Diels-Alder reactions, from three linezolid analogs containing morpholine, piperazine and thiomorpholine, respectively, as the C-ring components. Subsequent N-O bond cleavage generated oxazolidinones with 4-amino cyclo-2-en-1-ol substituents. The in vitro antibacterial activities of these oxazolidinone analogs were evaluated. (C) 2009 Elsevier Ltd. All rights reserved.

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

 

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Product Details of 90-01-7, Chemistry graduates have much scope to use their knowledge in a range of research sectors, including roles within chemical engineering, chemical and related industries, healthcare and more.90-01-7, Name is Salicyl Alcohol, SMILES is C1=CC=CC(=C1O)CO, belongs to thiomorpholine compound. In a article, author is Yan, Shanshan, introduce new discover of the category.

A series of novel oxazolidinone antibiotics having [2.2.1] and [2.2.2] bicyclic oxazine moieties at the C-5 side chain of the A-ring was synthesized by nitroso Diels-Alder reactions, from three linezolid analogs containing morpholine, piperazine and thiomorpholine, respectively, as the C-ring components. Subsequent N-O bond cleavage generated oxazolidinones with 4-amino cyclo-2-en-1-ol substituents. The in vitro antibacterial activities of these oxazolidinone analogs were evaluated. (C) 2009 Elsevier Ltd. All rights reserved.

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

 

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Reference of 90-01-7, New discoveries in chemical research and development in 2021.The transformation of simple hydrocarbons into more complex and valuable products via catalytic C–H bond functionalisation has revolutionised modern synthetic chemistry. 90-01-7, Name is Salicyl Alcohol, SMILES is C1=CC=CC(=C1O)CO, molecular formula is C7H8O2, belongs to thiomorpholine compound. In an article, author is Mancy, Ahmed, introduce new discover of the category.

Bacterial resistance to antibiotics is presently one of the most pressing healthcare challenges and necessitates the discovery of new antibacterials with unique chemical scaffolds. However, the determination of the optimal balance between structural requirements for pharmacological action and pharmacokinetic properties of novel antibacterial compounds is a significant challenge in drug development. The incorporation of lipophilic moieties within a compound’s core structure can enhance biological activity but have a deleterious effect on drug-like properties. In this Article, the lipophilicity of alkynylphenylthiazoles, previously identified as novel antibacterial agents, was reduced by introducing cyclic amines to the lipophilic side chain. In this regard, substitution with methylpiperidine (compounds 14-16) and thiomorpholine (compound 19) substituents significantly enhanced the aqueous solubility profile of the new compounds more than 150-fold compared to the first-generation lead compound 1b. Consequently, the pharmacokinetic profile of compound 15 was significantly enhanced with a notable improvement in both half-life and the time the compound’s plasma concentration remained above its minimum inhibitory concentration (MIC) against methicillin-resistant Staphylococcus aureus (MRSA). In addition, compounds 14-16 and 19 were found to exert a bactericidal mode of action against MRSA and were not susceptible to resistance formation after 14 serial passages. Moreover, these compounds (at 2X MIC) were superior to the antibiotic vancomycin in the disruption of the mature MRSA biofilm. The modifications to the alkynylphenylthiazoles reported herein successfully improved the pharmacokinetic profile of this new series while maintaining the compounds’ biological activity against MRSA.

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

 

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Substituted anilines and vinyl sulfone undergo a facile double Michael addition to form substituted phenylthiomorpholine dioxide, catalyzed with AlCl3 or H3PO4. Scope and conditions were explored. (C) 2003 Elsevier Science Ltd. All rights reserved.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

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The behavior of a non-incinerative reductive thermal cocurrent flow gasification process (ChemChar Process) when used to treat representative sulfur compounds is reported. Gasification of 1,3-benzenedisulfonic acid, thiomorpholine, and sulfuric acid converts the sulfur in these compounds to H2S, OCS, and elemental sulfur. The H2S and OCS are released in the synthesis with the gas product from which they can be scrubbed, with the elemental sulfur being deposited on the char matrix. No production of sulfur dioxide was detected. Gasified sulfur products recovered amounted to 89-114% of the total sulfur present in the sulfur compounds gasified, although exact mass balances could not be obtained due to the sulfur present in the char. (C) 1998 Elsevier Science Ltd. All rights reserved.

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Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem

 

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A series of novel oxazolidinone antibiotics having [2.2.1] and [2.2.2] bicyclic oxazine moieties at the C-5 side chain of the A-ring was synthesized by nitroso Diels-Alder reactions, from three linezolid analogs containing morpholine, piperazine and thiomorpholine, respectively, as the C-ring components. Subsequent N-O bond cleavage generated oxazolidinones with 4-amino cyclo-2-en-1-ol substituents. The in vitro antibacterial activities of these oxazolidinone analogs were evaluated. (C) 2009 Elsevier Ltd. All rights reserved.

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