N-(1-ethynylcyclohexyl)-4-methylbenzenesulfonamide

Base Information

Chemical Name:N-(1-ethynylcyclohexyl)-4-methylbenzenesulfonamide
CAS No.:126583-98-0
Molecular Formula:C15H19NO2S
Molecular Weight:277.387
Hs Code.:
DSSTox Substance ID:DTXSID80395805
Wikidata:Q82196101
Mol file:126583-98-0.mol

Synonyms:N-(1-ethynylcyclohexyl)-4-methylbenzenesulfonamide;126583-98-0;N-(1-ethynylcyclohexyl)-4-methylbenzene-1-sulfonamide;DTXSID80395805;MFCD05670168;AKOS005110801;MS-2772

Suppliers and Price of N-(1-ethynylcyclohexyl)-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 2 raw suppliers

Chemical Property of N-(1-ethynylcyclohexyl)-4-methylbenzenesulfonamide

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:277.11365002
Heavy Atom Count:19
Complexity:440

Purity/Quality:: 85.0-99.8% ^*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)NC2(CCCCC2)C#C

Technology Process of N-(1-ethynylcyclohexyl)-4-methylbenzenesulfonamide

There total 1 articles about N-(1-ethynylcyclohexyl)-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: 89.0%

: 30389-18-5
1-Ethynylcyclohexylamine

: 98-59-9
p-toluenesulfonyl chloride

: 126583-98-0
N-(1-ethynylcyclohexyl)-4-methyl-benzenesulfonamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/acs.orglett.9b02446

Reference yield: 99.0%

: 126583-98-0
N-(1-ethynylcyclohexyl)-4-methyl-benzenesulfonamide

: 563-47-3
3-Chloro-2-methylpropene

: 491879-40-4
N-(1-ethynylcyclohexyl)-4-methyl-N-(2-methylallyl)benzenesulfonamide

Guidance literature:: N-(1-ethynylcyclohexyl)-4-methyl-benzenesulfonamide; With sodium hydride; In tetrahydrofuran; N,N-dimethyl-formamide; at 0 ℃;

3-Chloro-2-methylpropene; With sodium iodide; In tetrahydrofuran; N,N-dimethyl-formamide; at 20 ℃; Further stages.;
DOI:10.1002/1615-4169(200208)344:6/7<678::AID-ADSC678>3.0.CO;2-P

Reference yield: 98.0%

: 126583-98-0
N-(1-ethynylcyclohexyl)-4-methyl-benzenesulfonamide

: 491879-40-4
N-(1-ethynylcyclohexyl)-4-methyl-N-(2-methylallyl)benzenesulfonamide

Guidance literature:: With tetra-(n-butyl)ammonium iodide; potassium carbonate; In acetone; at 60 ℃; Inert atmosphere;
DOI:10.1021/acs.orglett.6b01901