N-Tosylindole

Base Information

Chemical Name:N-Tosylindole
CAS No.:31271-90-6
Molecular Formula:C15H13NO2S
Molecular Weight:271.34
Hs Code.:2933990090
DSSTox Substance ID:DTXSID50449788
Nikkaji Number:J502.184G
Wikidata:Q27461675
ChEMBL ID:CHEMBL1084600
Mol file:31271-90-6.mol

Synonyms:N-tosylindole

Suppliers and Price of N-Tosylindole

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

AOBChem
1-[(4-Methylphenyl)sulfonyl]-1H-indole 97%
10g
$ 196.00

American Custom Chemicals Corporation
1-(P-TOLUENESULFONYL)INDOLE 95.00%
5MG
$ 497.60

Alfa Aesar
1-(p-Toluenesulfonyl)indole, 95%
5g
$ 192.00

Alfa Aesar
1-(p-Toluenesulfonyl)indole, 95%
1g
$ 57.00

Alfa Aesar
1-(p-Toluenesulfonyl)indole, 95%
25g
$ 544.00

aablocks
1-(P-Toluenesulfonyl)indole 95%
25g
$ 734.00

aablocks
1-(P-Toluenesulfonyl)indole 95%
5g
$ 284.00

Total 20 raw suppliers

Chemical Property of N-Tosylindole

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:84-86 °C
Refractive Index:1.627
Boiling Point:458.269 °C at 760 mmHg
Flash Point:230.953 °C
PSA：47.45000
Density:1.24 g/cm³
LogP:4.26750
Storage Temp.:Sealed in dry,Room Temperature
Water Solubility.:Insoluble in water.
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:271.06669983
Heavy Atom Count:19
Complexity:406

Purity/Quality:

98%Min ^*data from raw suppliers

1-[(4-Methylphenyl)sulfonyl]-1H-indole 97% ^*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=CC=CC=C32
Uses 1-(p-Toluenesulfonyl)indole, is synthesized and used as a stable equivalent of 4-mercaptoindoles, also used in medicinal field for making drug and tablets.

Technology Process of N-Tosylindole

There total 91 articles about N-Tosylindole 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: 100.0%

: 527686-25-5
4-methyl-N-(2-((trimethylsilyl)ethynyl)phenyl)benzenesulfonamide

: 31271-90-6
1-(p-toluenesulfonyl)-1H-indole

Guidance literature:: With potassium carbonate; In water; at 130 ℃; for 10h; Sealed tube; Inert atmosphere;
DOI:10.1016/j.cclet.2016.07.022

Reference yield: 100.0%

: 497236-62-1
N-(2-ethynylphenyl)-4-toluenesulfonamide

: 31271-90-6
1-(p-toluenesulfonyl)-1H-indole

Guidance literature:: With potassium carbonate; In water; at 130 ℃; for 10h; Sealed tube; Inert atmosphere;
DOI:10.1016/j.cclet.2016.07.022

Reference yield: 99.0%

: 120-72-9
indole

: 98-59-9
p-toluenesulfonyl chloride

: 31271-90-6
1-(p-toluenesulfonyl)-1H-indole

Guidance literature:: indole; With sodium hydride; In acetonitrile; at 0 ℃; for 0.166667h;

p-toluenesulfonyl chloride; In acetonitrile; at 0 - 20 ℃; for 4h;
DOI:10.1021/acs.jafc.8b00507