1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)-

Base Information

Chemical Name:1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)-
CAS No.:85953-39-5
Molecular Formula:C14H10ClNO4S2
Molecular Weight:355.81700
Hs Code.:
DSSTox Substance ID:DTXSID70558088
Wikidata:Q82440234

Synonyms:85953-39-5;1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)-;1-(Phenylsulfonyl)-1H-indole-2-sulfonyl chloride;1-(Benzenesulfonyl)-1H-indole-2-sulfonyl chloride;1-(BENZENESULFONYL)INDOLE-2-SULFONYL CHLORIDE;SCHEMBL6735824;DTXSID70558088;VBZLCEHJLXBBHR-UHFFFAOYSA-N;BS-52769;1-phenylsulfonyl-1H-indole-2-sulfonyl chloride;E75548;EN300-22808458;1-BENZENESULFONYL-1H-INDOLE-2-SULFONYL CHLORIDE

Suppliers and Price of 1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)-

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

Ambeed
1-(Phenylsulfonyl)-1H-indole-2-sulfonylchloride 97%
5g
$ 526.00

Ambeed
1-(Phenylsulfonyl)-1H-indole-2-sulfonylchloride 97%
1g
$ 178.00

Ambeed
1-(Phenylsulfonyl)-1H-indole-2-sulfonylchloride 97%
250mg
$ 90.00

Total 4 raw suppliers

Chemical Property of 1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)-

Chemical Property:

Melting Point:118-120 °C
Boiling Point:562.6±42.0 °C(Predicted)
PSA：89.97000
Density:1.52±0.1 g/cm3(Predicted)
LogP:4.96740
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:354.9739778
Heavy Atom Count:22
Complexity:602

Purity/Quality:

99% ^*data from raw suppliers

1-(Phenylsulfonyl)-1H-indole-2-sulfonylchloride 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)S(=O)(=O)N2C3=CC=CC=C3C=C2S(=O)(=O)Cl

Technology Process of 1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)-

There total 8 articles about 1H-Indole-2-sulfonyl chloride, 1-(phenylsulfonyl)- 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:

: 1394431-02-7
lithium 1-(phenylsulfonyl)-1H-indole-2-sulfinate

: 85953-39-5
1-phenylsulfonyl-1H-indole-2-sulfonyl chloride

Guidance literature:: With N-chloro-succinimide; In dichloromethane; at 5 ℃; for 2h;
DOI:10.1016/j.bmcl.2016.08.018

Reference yield:

: 40899-71-6
1-benzenesulfonylindole

: 85953-39-5
1-phenylsulfonyl-1H-indole-2-sulfonyl chloride

Guidance literature:: Multistep reaction;
DOI:10.1021/jm00164a045

Reference yield:

: 120-72-9
indole

: 85953-39-5
1-phenylsulfonyl-1H-indole-2-sulfonyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) 1.6 M n-butyllithium / 1.) THF, hexane, from -70 deg C to 0 deg C, 45 min, 2.) from -70 deg C to room temperature, 2 h

With n-butyllithium;
DOI:10.1021/jm00164a045