N-Cyclopentylidene-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-Cyclopentylidene-4-methylbenzenesulfonamide
CAS No.:118616-82-3
Molecular Formula:C₁₂H₁₅NO₂S
Molecular Weight:237.323
Hs Code.:
DSSTox Substance ID:DTXSID30556106
Mol file:118616-82-3.mol

Synonyms:118616-82-3;N-Cyclopentylidene-4-methylbenzenesulfonamide;Benzenesulfonamide, N-cyclopentylidene-4-methyl- (9CI);DTXSID30556106;N-Cyclopentylidene-4-methylbenzene-1-sulfonamide;Benzenesulfonamide,N-cyclopentylidene-4-methyl-(9ci)

Suppliers and Price of N-Cyclopentylidene-4-methylbenzenesulfonamide

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

Total 3 raw suppliers

Chemical Property of N-Cyclopentylidene-4-methylbenzenesulfonamide

Chemical Property:

PSA：54.88000
LogP:3.77950
XLogP3:2.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:237.08234989
Heavy Atom Count:16
Complexity:351

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)S(=O)(=O)N=C2CCCC2

Technology Process of N-Cyclopentylidene-4-methylbenzenesulfonamide

There total 2 articles about N-Cyclopentylidene-4-methylbenzenesulfonamide 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:

: 6873-55-8
p-tolylsulfinyl amide

: 120-92-3
cyclopentanone

: 118616-82-3
N-Cyclopentylidene-4-methyl-benzenesulfonamide

Guidance literature:: p-tolylsulfinyl amide; cyclopentanone;

With 3-chloro-benzenecarboperoxoic acid;
DOI:10.1080/00397911.2011.594974

Reference yield:

: 10439-23-3
4-methylbenzenesulfinyl chloride

: 1192-28-5
Cyclopentanone oxime

: 118616-82-3
N-Cyclopentylidene-4-methyl-benzenesulfonamide

Guidance literature:: With triethylamine; Multistep reaction; 1.) Et₂O, -15 degC, 10 min; 2.) r.t., 1 h;
DOI:10.1039/c39880000931

Reference yield: 86.0%

: 94111-03-2
3-acetoxy-3-cyano-2-trimethylsilylmethylpropene

: 118616-82-3
N-Cyclopentylidene-4-methyl-benzenesulfonamide

: 1231765-35-7
(R)-3-methylene-1-tosyl-1-azaspiro[4.4]nonane-4-carbonitrile

Guidance literature:: With O,O'-(R)-(1,1'-dinaphthyl-2,2'-diyl)-N-((R,R)-2,5-di(naphthyl)pyrrolidine); allyl(cyclopentadiene)palladium(II); In toluene; at 4 ℃; optical yield given as %ee; enantioselective reaction;
DOI:10.1021/ja102102d