1H-Indole-2-sulfonamide

Base Information

Chemical Name:1H-Indole-2-sulfonamide
CAS No.:85953-41-9
Molecular Formula:C₈H₈N₂O₂S
Molecular Weight:196.23
Hs Code.:
ChEMBL ID:CHEMBL162064
DSSTox Substance ID:DTXSID30558089
Nikkaji Number:J273.555E
Pharos Ligand ID:RD683T7JMU4S
Wikidata:Q82440237
Mol file:85953-41-9.mol

Synonyms:1H-INDOLE-2-SULFONAMIDE;85953-41-9;CHEMBL162064;indolesulfonamide;indole sulfonamide;1H-Indole-2-sulfonic acid amide;SCHEMBL32895;DTXSID30558089;RYMYQAMZUWJAEO-UHFFFAOYSA-N;BDBM50406338;MFCD18809113;BS-51052;E76678;EN300-1989103

Suppliers and Price of 1H-Indole-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

AccelPharmtech
1H-Indole-2-sulfonamide 97.00%
25G
$ 6000.00

AccelPharmtech
1H-Indole-2-sulfonamide 97.00%
5G
$ 3230.00

AccelPharmtech
1H-Indole-2-sulfonamide 97.00%
1G
$ 1890.00

Total 5 raw suppliers

Chemical Property of 1H-Indole-2-sulfonamide

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:196.03064868
Heavy Atom Count:13
Complexity:283

Purity/Quality:

99%, ^*data from raw suppliers

1H-Indole-2-sulfonamide 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=C(N2)S(=O)(=O)N

Technology Process of 1H-Indole-2-sulfonamide

There total 5 articles about 1H-Indole-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: 90.0%

: 120-72-9
indole

: 85953-41-9
1H-indole-2-sulfonamide

Guidance literature:: indole; With n-butyllithium; carbon monoxide; at -78 - 20 ℃;

With sulfur dioxide; tert.-butyl lithium; at -78 - 20 ℃;

With sodium acetate; hydroxylamine-O-sulfonic acid; In water; Further stages.;
DOI:10.1016/j.tetlet.2007.10.046

Reference yield:

: 85953-40-8
1-(phenylsulfonyl)indole-2-sulfonamide

: 85953-41-9
1H-indole-2-sulfonamide

Guidance literature:: With sodium hydroxide; at 80 ℃; for 0.5h;
DOI:10.1021/jm00164a045

Reference yield:

: 40899-71-6
1-benzenesulfonylindole

: 85953-41-9
1H-indole-2-sulfonamide

Guidance literature:: Multi-step reaction with 3 steps

2: NH₃ (gas) / tetrahydrofuran / 5 °C

3: 10percent NaOH / 0.5 h / 80 °C

With sodium hydroxide; ammonia; In tetrahydrofuran;
DOI:10.1021/jm00164a045