1-Tosyl-2-methyl-1H-indole

Base Information

Chemical Name:1-Tosyl-2-methyl-1H-indole
CAS No.:173436-68-5
Molecular Formula:C16H15NO2S
Molecular Weight:285.367
Hs Code.:
DSSTox Substance ID:DTXSID701244907
Nikkaji Number:J701.760J

Synonyms:N-tosyl-2-methylindole;1-Tosyl-2-methyl-1H-indole;DTXSID701244907;2-Methyl-1-[(4-methylphenyl)sulfonyl]-1H-indole;173436-68-5

Suppliers and Price of 1-Tosyl-2-methyl-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
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Total 0 raw suppliers

Chemical Property of 1-Tosyl-2-methyl-1H-indole

Chemical Property:

XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:285.08234989
Heavy Atom Count:20
Complexity:434

Purity/Quality:

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)C

Technology Process of 1-Tosyl-2-methyl-1H-indole

There total 47 articles about 1-Tosyl-2-methyl-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: 92.0%

: 51315-69-6
N-tosyl-o-allylaniline

: 173436-68-5
2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-indole

Guidance literature:: With potassium fluoride; oxygen; palladium diacetate; acetic acid; Reagent/catalyst;
DOI:10.1007/s00706-016-1819-2

Reference yield: 91.1%

: 758686-23-6
N-[2-(prop-1-yn-1-yl)phenyl]-p-toluenesulfonamide

: 173436-68-5
2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-indole

Guidance literature:: With caesium carbonate; copper(l) chloride; In acetonitrile; at 20 ℃; for 6h; under 760.051 Torr;

Reference yield: 83.0%

: 75-36-5
acetyl chloride

: 243844-35-1
N-[2-(chloromethyl)-phenyl]-4-methylbenzene-1-sulfonamide

: 173436-68-5
2-methyl-1-[(4-methylphenyl)sulfonyl]-1H-indole

Guidance literature:: With caesium hydroxide monohydrate; triphenylphosphine; In dichloromethane; at 25 ℃; for 72h; Schlenk technique;
DOI:10.1002/adsc.202000343