1H-Indole, 1-(phenylsulfonyl)-2-(2-propenyl)-

Base Information Edit

Chemical Name:1H-Indole, 1-(phenylsulfonyl)-2-(2-propenyl)-
CAS No.:112475-54-4
Molecular Formula:C17H15NO2S
Molecular Weight:297.378
Hs Code.:
DSSTox Substance ID:DTXSID60438688
Nikkaji Number:J656.657J
Wikidata:Q82254500
Mol file:112475-54-4.mol

Synonyms:1H-Indole, 1-(phenylsulfonyl)-2-(2-propenyl)-;112475-54-4;DTXSID60438688;1-Phenylsulfonyl-2-allyl-1H-indole

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

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1H-Indole, 1-(phenylsulfonyl)-2-(2-propenyl)- Edit

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:297.08234989
Heavy Atom Count:21
Complexity:462

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCC1=CC2=CC=CC=C2N1S(=O)(=O)C3=CC=CC=C3

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

There total 2 articles about 1H-Indole, 1-(phenylsulfonyl)-2-(2-propenyl)- 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: 74.0%

: 40899-71-6
1-benzenesulfonylindole

: 106-95-6
allyl bromide

: 112475-54-4
N-phenylsulphonyl-2-allylindole

Guidance literature:: 1-benzenesulfonylindole; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; Inert atmosphere;

allyl bromide; In tetrahydrofuran; hexane; at -78 - -50 ℃; Inert atmosphere;
DOI:10.1021/jo9009497

Reference yield:

: 99275-44-2
2-iodo-1-(phenylsulfonyl)-1H-indole

: 106-95-6
allyl bromide

: 112475-54-4
N-phenylsulphonyl-2-allylindole

Guidance literature:: With N,N,N,N,-tetramethylethylenediamine; methyllithium; zinc(II) chloride; Yield given. Multistep reaction; 1.) Et₂O, THF, -78 deg C, 1 h, 2.) -78 deg C to room temperature, 12 h;