3-Methanesulfonyloxy-benzoic acid methyl ester

Base Information

Chemical Name:3-Methanesulfonyloxy-benzoic acid methyl ester
CAS No.:161912-35-2
Molecular Formula:C9H10O5S
Molecular Weight:230.241
Hs Code.:
DSSTox Substance ID:DTXSID60440024
Nikkaji Number:J2.292.698E
Wikidata:Q82256170
Mol file:161912-35-2.mol

Synonyms:3-methanesulfonyloxy-benzoic acid methyl ester;161912-35-2;SCHEMBL2962698;DTXSID60440024;PZCKUKUFDUITMF-UHFFFAOYSA-N;3-(Mesyloxy)benzoic acid methyl ester;METHYL 3-(METHANESULFONYLOXY)BENZOATE

Suppliers and Price of 3-Methanesulfonyloxy-benzoic acid methyl ester

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 3-Methanesulfonyloxy-benzoic acid methyl ester

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:230.02489459
Heavy Atom Count:15
Complexity:316

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C1=CC(=CC=C1)OS(=O)(=O)C

Technology Process of 3-Methanesulfonyloxy-benzoic acid methyl ester

There total 4 articles about 3-Methanesulfonyloxy-benzoic acid methyl ester 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: 94.0%

: 19438-10-9
methyl 3-hydroxybenzoate

: 124-63-0
methanesulfonyl chloride

: 161912-35-2
methyl 3-((methylsulfonyl)oxy)benzoate

Guidance literature:: With triethylamine; at 20 ℃; for 20h;
DOI:10.1002/chem.200601184

Reference yield: 91.0%

: 67-56-1
methanol

: 15226-74-1,61091-28-9,61117-58-6
dicobalt octacarbonyl

: C₁₃H₇F₅O₆S₂

: 161912-35-2
methyl 3-((methylsulfonyl)oxy)benzoate

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; at 20 ℃; for 16h; chemoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/adsc.201600736

Reference yield: 87.0%

: 67-56-1
methanol

: 15226-74-1,61091-28-9,61117-58-6
dicobalt octacarbonyl

: C₈H₇F₃O₆S₂

: 161912-35-2
methyl 3-((methylsulfonyl)oxy)benzoate

Guidance literature:: With dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; potassium acetate; at 20 ℃; for 16h; chemoselective reaction; Schlenk technique; Inert atmosphere;
DOI:10.1002/adsc.201600736