6-Chloro-1-tosyl-1H-indole

Base Information

Chemical Name:6-Chloro-1-tosyl-1H-indole
CAS No.:31271-88-2
Molecular Formula:C15H12ClNO2S
Molecular Weight:305.785
Hs Code.:2933990090
DSSTox Substance ID:DTXSID80459951
Wikidata:Q82283844
Mol file:31271-88-2.mol

Synonyms:6-Chloro-1-tosyl-1H-indole;31271-88-2;SCHEMBL1306928;DTXSID80459951;PDTINBYILVIGEO-UHFFFAOYSA-N;6-chloro-1-(toluene-4-sulfonyl)-1h-indole;6-chloro-1-(4-methylbenzenesulfonyl)-1H-indole

Suppliers and Price of 6-Chloro-1-tosyl-1H-indole

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

Crysdot
6-Chloro-1-tosyl-1H-indole 95+%
1g
$ 772.00

Chemenu
6-chloro-1-tosyl-1H-indole 95%
1g
$ 729.00

American Custom Chemicals Corporation
6-CHLORO-1-TOSYL-1H-INDOLE 95.00%
5MG
$ 495.94

Alichem
6-Chloro-1-tosyl-1H-indole
1g
$ 634.28

Total 6 raw suppliers

Chemical Property of 6-Chloro-1-tosyl-1H-indole

Chemical Property:

PSA：47.45000
LogP:4.92090
Storage Temp.:2-8°C
XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:305.0277275
Heavy Atom Count:20
Complexity:439

Purity/Quality:

99% ^*data from raw suppliers

6-Chloro-1-tosyl-1H-indole 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N2C=CC3=C2C=C(C=C3)Cl

Technology Process of 6-Chloro-1-tosyl-1H-indole

There total 9 articles about 6-Chloro-1-tosyl-1H-indole 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: 91.0%

: 17422-33-2
6-chloroindole

: 98-59-9
p-toluenesulfonyl chloride

: 31271-88-2
6-chloro-N-p-tolylsulfonylindole

Guidance literature:: With N-benzyl-N,N,N-triethylammonium chloride; sodium hydroxide; In dichloromethane; at 20 ℃; for 16h;
DOI:10.1021/acs.oprd.8b00248

Reference yield: 85.0%

: 6-chloro-1-tosylindoline-2,3-dione

: 1616975-14-4
N-(p-toluenesulfonyl)-6-chloroindolinone

: 31271-88-2
6-chloro-N-p-tolylsulfonylindole

Guidance literature:: With tris(pentafluorophenyl)borate; benzyldimethylsilane; In 1,2-dichloro-benzene; at 120 ℃; for 72h; chemoselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.0c03150

Reference yield: 82.0%

: 2-(2,4-dichlorophenyl)-1-tosylaziridine

: 31271-88-2
6-chloro-N-p-tolylsulfonylindole

Guidance literature:: 2-(2,4-dichlorophenyl)-1-tosylaziridine; With boron trifluoride diethyl etherate; thiophenol; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;

With copper; In dichloromethane; N,N-dimethyl-formamide; at 120 ℃; for 16h; Inert atmosphere;
DOI:10.1021/acs.joc.5b02251