N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide

Base Information

Chemical Name:N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide
CAS No.:216578-30-2
Molecular Formula:C12H15 N O2 S
Molecular Weight:237.318
Hs Code.:
DSSTox Substance ID:DTXSID60460545
Nikkaji Number:J997.209I
Mol file:216578-30-2.mol

Synonyms:216578-30-2;N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide;N-cyclopent-3-en-1-yl-4-methylbenzenesulfonamide;N-(Cyclopent-3-en-1-yl)-4-methylbenzenesulfonamide;N-Cyclopent-3-enyl-4-methyl-benzenesulfonamide;N-(3-Cyclopenten-1-yl)-4-methylbenzenesulfonamide;Benzenesulfonamide, N-3-cyclopenten-1-yl-4-methyl- (9CI);DTXSID60460545

Suppliers and Price of N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide

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 9 raw suppliers

Chemical Property of N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide

Chemical Property:

PSA：54.55000
LogP:3.46360
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:237.08234989
Heavy Atom Count:16
Complexity:340

Purity/Quality:: 1%-101.0% ^*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)NC2CC=CC2

Technology Process of N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide

There total 8 articles about N-(Cyclopent-3-en-1-yl)-4-methylbenzene-1-sulfonamide 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%

: 91469-55-5
cyclopent-3-en-1-amine hydrogen chloride

: 216578-30-2
4-(4-methylbenzenesulfonamido)cyclopentene

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/S0040-4039(98)01821-8

Reference yield: 79.0%

: 172791-01-4
6-(toluene-4-sulfonyl)-6-aza-bicyclo[3.1.0]hex-2-ene

: 216578-30-2
4-(4-methylbenzenesulfonamido)cyclopentene

Guidance literature:: With lithium triethylborohydride; In tetrahydrofuran; at 0 ℃; for 1h;
DOI:10.1016/S0040-4039(01)02238-9

Reference yield:

: 55962-05-5
[N-(p-tolylsulfonyl)imino]phenyliodinane

: 216578-30-2
4-(4-methylbenzenesulfonamido)cyclopentene

Guidance literature:: Multi-step reaction with 2 steps

1: 88 percent / Cu(acac)2 / acetonitrile / 1 h / 0 - 20 °C

2: 79 percent / LiEt₃BH / tetrahydrofuran / 1 h / 0 °C

With lithium triethylborohydride; copper acetylacetonate; In tetrahydrofuran; acetonitrile;
DOI:10.1016/S0040-4039(01)02238-9