Chemistry, like all the natural sciences, HPLC of Formula: C8H8O2, begins with the direct observation of nature¡ª in this case, of matter.135-02-4, Name is 2-Methoxybenzaldehyde, SMILES is O=CC1=CC=CC=C1OC, belongs to thiomorpholine compound. In a document, author is Pulipati, Lokesh, introduce the new discover.
Click-based synthesis and antitubercular evaluation of novel dibenzo [b,d]thiophene-1,2,3-triazoles with piperidine, piperazine, morpholine and thiomorpholine appendages
A series of novel piperidine, piperazine, morpholine and thiomorpholine appended dibenzo[b,d] thiophene-1,2,3-triazoles were designed and synthesized utilizing azide-alkyne click chemistry in the penultimate step. The required azide building block 6a-e was synthesized from commercial dibenzo[b, d] thiophene in good yields following five step reaction sequence. All the new analogues 8a-f, 9a-f, 10a-f, 11a-f & 12a-f were characterized by their NMR and mass spectral analysis. Screening all thirty new compounds for in vitro antimycobacterial activity against Mycobacterium tuberculosis H37Rv, resulted 8a, 8f and 11e as potent analogues with MIC 0.78 mu g/mL, 0.78 mu g/mL & 1.56 mu g/mL, respectively, and has shown lower cytotoxicity. Interestingly, all six piperazine appended dibenzo[b, d] thiophene-1,2,3-triazoles 11a-f exhibited Mtb inhibition activity with MIC 1.56-12.5 mu g/mL. To some extent, the data observed here indicated Mycobacterium tuberculosis inhibition among the appendages is in the order, piperazine > thiomorpholine > morpholine. (C) 2016 Elsevier Ltd. All rights reserved.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions. you can also check out more blogs about 135-02-4. HPLC of Formula: C8H8O2.
Reference:
Thiomorpholine – Wikipedia,
,Thiomorpholine | C4H9NS – PubChem