2-Methylprop-2-ene-1-sulfonyl chloride

Base Information

Chemical Name:2-Methylprop-2-ene-1-sulfonyl chloride
CAS No.:14568-34-4
Molecular Formula:C4H7ClO2S
Molecular Weight:154.617
Hs Code.:
European Community (EC) Number:970-396-6
Nikkaji Number:J2.001.555A
Mol file:14568-34-4.mol

Synonyms:2-methylprop-2-ene-1-sulfonyl chloride;14568-34-4;SCHEMBL10499156;DWAZFVPADZFXAQ-UHFFFAOYSA-;2-methylprop-2-ene-1-sulfonylchloride;AKOS006334238;CS-0235086;EN300-152591;InChI=1/C4H7ClO2S/c1-4(2)3-8(5,6)7/h1,3H2,2H3

Suppliers and Price of 2-Methylprop-2-ene-1-sulfonyl chloride

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 4 raw suppliers

Chemical Property of 2-Methylprop-2-ene-1-sulfonyl chloride

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:153.9855283
Heavy Atom Count:8
Complexity:175

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=C)CS(=O)(=O)Cl

Technology Process of 2-Methylprop-2-ene-1-sulfonyl chloride

There total 1 articles about 2-Methylprop-2-ene-1-sulfonyl chloride 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: 79.0%

: 1561-92-8
sodium methallylsulfonate

: 101-54-2
N-phenylphenylene-1,4-diamine

: N-(4-anilino)phenylisopropenylsulfonamide

: 14568-34-4
2-methylprop-2-ene-1-sulfonyl chloride

Guidance literature:: With phosphorus pentachloride; triethylamine;

Reference yield: 87.0%

: 14568-34-4
2-methylprop-2-ene-1-sulfonyl chloride

: 13139-86-1
4-methoxyphenyl magnesium bromide

: 20849-82-5
1-methoxy-4-(2-methylallyl)benzene

Guidance literature:: With iron(III) acetylacetonate; In tetrahydrofuran; at 25 ℃; for 3h; Inert atmosphere;
DOI:10.1002/ejoc.200900927

Reference yield: 87.0%

: 14568-34-4
2-methylprop-2-ene-1-sulfonyl chloride

: 33872-80-9
o-tolyl magnesium chloride

: 188404-16-2
1-methyl-2-(2-methyl-2-propenyl)benzene

Guidance literature:: With bis(tri-t-butylphosphine)palladium⁽⁰⁾; In tetrahydrofuran; at 25 ℃; for 0.5h; regioselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2008.11.007