Thiophene-3-sulfonamide

Base Information

• Chemical Name: Thiophene-3-sulfonamide
• CAS No.: 64255-63-6
• Molecular Formula: C4H5 N O2 S2
• Molecular Weight: 163.221
• Hs Code.: 2935009090
• DSSTox Substance ID: DTXSID30360881
• Wikidata: Q82142895
• Mol file: 64255-63-6.mol

Synonyms:thiophene-3-sulfonamide;64255-63-6;3-THIOPHENESULFONAMIDE;3-Thiophenesulfonamide(7CI,9CI);SCHEMBL1035591;DTXSID30360881;BWJZHYWAXLWLTB-UHFFFAOYSA-N;MFCD03426807;AKOS006279484;AT34951;CS-0222468;EN300-111227;AP-836/41220357;Z1198162755

Chemical Property of Thiophene-3-sulfonamide

Chemical Property:

• PSA: 96.78000
• LogP: 2.17660
• XLogP3: 0.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 162.97617075
• Heavy Atom Count: 9
• Complexity: 181

Purity/Quality:

98% ^*data from raw suppliers

thiophene-3-sulfonamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CSC=C1S(=O)(=O)N

Technology Process of Thiophene-3-sulfonamide

There total 1 articles about Thiophene-3-sulfonamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

thifensulfuron methyl (79277-27-3) → Thiophene-3-sulfonamide (64255-63-6) + 2-(methoxycarbonyl)thiophene-3-sulfonic acid (59337-96-1) + 4-methoxy-6-methyl-1,3,5-triazin-2-amine (1668-54-8) + N-(4-methoxy-6-methyl-1,3,5-triazin-2-yl) urea (208252-67-9)

Guidance literature:

With oxygen; In water; at 20 ℃; pH=7; pH-value; Kinetics; Quantum yield; Mechanism; Photolysis;

DOI:10.1016/j.jphotochem.2009.11.017

Reference yield:

Thiophene-3-sulfonamide (64255-63-6) + p-chlorphenylisocyanate (104-12-1) → N-[[(4-chlorophenyl)amino]carbonyl]-3-thiophenesulfonamide

Guidance literature:

With hydrogenchloride; In acetone;

Reference yield:

Thiophene-3-sulfonamide (64255-63-6) + 2,4 dichlorobenzoic acid (50-84-0) → thiophene-3-sulfonic acid 2,4-dichloro-benzoylamide

Guidance literature:

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃;

DOI:10.1016/j.bmcl.2004.11.041

upstream raw materials:

thifensulfuron methyl

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