Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

Base Information

Chemical Name:Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide
CAS No.:90141-25-6
Molecular Formula:C₁₆H₁₄N₂O₄S
Molecular Weight:330.364
Hs Code.:
DSSTox Substance ID:DTXSID60368057
Wikidata:Q82154343
Mol file:90141-25-6.mol

Synonyms:Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide;90141-25-6;N-(4-Sulfamoylbenzyl)benzofuran-2-carboxamide;N-[(4-sulfamoylphenyl)methyl]-1-benzofuran-2-carboxamide;DTXSID60368057;AKOS007993757;EC-000.1679;benzo[b]furan-2-carboxylic acid 4-sulfamoylbenzylamide;Z30932166;N-[4-(aminosulfonyl)benzyl]-1-benzofuran-2-carboxamide;N-[4-(aminosulfonyl)benzyl]-1-benzo[b]furan-2-carboxamide

Suppliers and Price of Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

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
BENZOFURAN-2-CARBOXYLIC ACID 4-SULFAMOYL-BENZYLAMIDE 95.00%
5MG
$ 502.67

Total 3 raw suppliers

Chemical Property of Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

Chemical Property:

Refractive Index:1.657
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：114.27000
Density:1.397g/cm³
LogP:4.36610
XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:330.06742811
Heavy Atom Count:23
Complexity:523

Purity/Quality:: BENZOFURAN-2-CARBOXYLIC ACID 4-SULFAMOYL-BENZYLAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C(O2)C(=O)NCC3=CC=C(C=C3)S(=O)(=O)N

Technology Process of Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

There total 4 articles about Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide 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: 70.0%

: 90141-23-4
4-{[(Benzofuran-2-carbonyl)-amino]-methyl}-benzenesulfonyl chloride

: 90141-25-6
Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

Guidance literature:: With ammonium hydroxide; for 2h;
DOI:10.1007/BF00765082

Reference yield:

: 41717-28-6
2-benzofuroyl chloride

: 90141-25-6
Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

Guidance literature:: Multi-step reaction with 3 steps

1: 60.5 percent / benzene / 5 h

2: 98.1 percent / chlorosulfuric acid / 2 h / -5 - -1 °C

3: 70 percent / aq. NH₃ / 2 h

With ammonium hydroxide; chlorosulphuric acid; In benzene;
DOI:10.1007/BF00765082

Reference yield:

: 100-46-9
benzylamine

: 90141-25-6
Benzofuran-2-carboxylic acid 4-sulfamoyl-benzylamide

Guidance literature:: Multi-step reaction with 3 steps

1: 60.5 percent / benzene / 5 h

2: 98.1 percent / chlorosulfuric acid / 2 h / -5 - -1 °C

3: 70 percent / aq. NH₃ / 2 h

With ammonium hydroxide; chlorosulphuric acid; In benzene;
DOI:10.1007/BF00765082