Fluoromethanesulfonyl chloride

Base Information

Chemical Name:Fluoromethanesulfonyl chloride
CAS No.:42497-69-8
Molecular Formula:CH2ClFO2S
Molecular Weight:132.543
Hs Code.:
European Community (EC) Number:816-406-3
DSSTox Substance ID:DTXSID70540928
Nikkaji Number:J3.324.843A
Wikidata:Q82417067
Mol file:42497-69-8.mol

Synonyms:fluoromethanesulfonyl chloride;42497-69-8;Fluoro-methanesulfonyl chloride;MFCD19200094;CH2ClFO2S;fluoromethanesulfonylchloride;SCHEMBL5778470;SCHEMBL7686497;DTXSID70540928;NNINWAWDVUHMGM-UHFFFAOYSA-N;AKOS006336255;AT12627;SB37155;BS-12672;SY041507;EN300-138820

Suppliers and Price of Fluoromethanesulfonyl 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

J&W Pharmlab
Fluoro-methanesulfonylchloride 96%
5g
$ 7998.00

J&W Pharmlab
Fluoro-methanesulfonylchloride 96%
1g
$ 1998.00

Crysdot
Fluoromethanesulfonylchloride 95%
250mg
$ 780.00

Total 10 raw suppliers

Chemical Property of Fluoromethanesulfonyl chloride

Chemical Property:

PSA：42.52000
LogP:1.56280
XLogP3:0.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:131.9448063
Heavy Atom Count:6
Complexity:110

Purity/Quality:

97% ^*data from raw suppliers

Fluoro-methanesulfonylchloride 96% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(F)S(=O)(=O)Cl
Uses Fluoromethanesulfony?l Chloride is a reagent used in the synthesis of N-Benzylacrylamides coupled with dearomatizing spirocyclization.

Technology Process of Fluoromethanesulfonyl chloride

There total 1 articles about Fluoromethanesulfonyl 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: 69.0%

: 98181-84-1
(4-chlorobenzyl)(fluoromethyl)sulfane

: 42497-69-8
monofluoromethylsulfonyl chloride

: 104-83-6
1-Chloro-4-(chloromethyl)benzene

Guidance literature:: With water; chlorine; In dichloromethane; at -5 ℃;

Reference yield: 68.0%

: 42497-69-8
monofluoromethylsulfonyl chloride

: 768-03-6,26742-84-7
Phenyl vinyl ketone

: 2-chloro-4-fluoro-1-phenylbutan-1-one

Guidance literature:: With dipotassium hydrogenphosphate; [Cu(2,9-bis(4-methoxyphenyl)-1,10-phenanthroline)₂]Cl; In 1,2-dichloro-ethane; at 20 ℃; Sealed tube; Inert atmosphere; Irradiation;
DOI:10.1002/anie.201412199

Reference yield: 67.0%

: 937-41-7
phenyl acrylate

: 42497-69-8
monofluoromethylsulfonyl chloride

: phenyl 2-chloro-4-fluorobutanoate

Guidance literature:: With dipotassium hydrogenphosphate; [Cu(2,9-bis(4-methoxyphenyl)-1,10-phenanthroline)₂]Cl; In 1,2-dichloro-ethane; at 20 ℃; Sealed tube; Inert atmosphere; Irradiation;
DOI:10.1002/anie.201412199