N-benzylthiophene-2-sulfonamide

Base Information

Chemical Name:N-benzylthiophene-2-sulfonamide
CAS No.:64255-65-8
Molecular Formula:C11H11NO2S2
Molecular Weight:253.346
Hs Code.:
DSSTox Substance ID:DTXSID50354181
Nikkaji Number:J3.576.850E
Wikidata:Q82132181
ChEMBL ID:CHEMBL1602388

Synonyms:N-benzylthiophene-2-sulfonamide;64255-65-8;Thiophene-2-sulfonic acid benzylamide;benzyl thiophene sulfonamide;Oprea1_076812;Oprea1_312275;MLS000067713;SCHEMBL7211477;CHEMBL1602388;DTXSID50354181;HMS1677P14;HMS2188C23;STL168311;AKOS000383449;WAY-302150;SMR000125056;CS-0235515;EN300-15763;Z45508785

Suppliers and Price of N-benzylthiophene-2-sulfonamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
THIOPHENE-2-SULFONIC ACID BENZYLAMIDE 95.00%
5MG
$ 499.48

Total 2 raw suppliers

Chemical Property of N-benzylthiophene-2-sulfonamide

Chemical Property:

PSA：82.79000
LogP:3.69830
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:253.02312094
Heavy Atom Count:16
Complexity:304

Purity/Quality:

99% ^*data from raw suppliers

THIOPHENE-2-SULFONIC ACID BENZYLAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CNS(=O)(=O)C2=CC=CS2

Technology Process of N-benzylthiophene-2-sulfonamide

There total 4 articles about N-benzylthiophene-2-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: 94.0%

: 308293-22-3
N-phenylmethylene 2-thiophenesulfonamide

: 64255-65-8
N-benzylthiophene-2-sulfonamide

Guidance literature:: With Schwartz's reagent; In dichloromethane; at 20 ℃; for 0.333333h; chemoselective reaction; Inert atmosphere; Schlenk technique;
DOI:10.1002/ejoc.201901607

Reference yield: 73.0%

: 6339-87-3
2-thiophensulfonamide

: 100-51-6,185532-71-2
benzyl alcohol

: 64255-65-8
N-benzylthiophene-2-sulfonamide

Guidance literature:: With [Mn(HN(C₂H₄PⁱPr₂)₂)(CO)₂Br]; potassium carbonate; In 5,5-dimethyl-1,3-cyclohexadiene; at 150 ℃; for 24h; Sealed tube;
DOI:10.1021/acs.joc.9b00203