Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl-

Base Information

Chemical Name:Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl-
CAS No.:134649-63-1
Molecular Formula:C12H16O5S
Molecular Weight:272.322
Hs Code.:
DSSTox Substance ID:DTXSID20447377
Nikkaji Number:J394.175B

Synonyms:134649-63-1;Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl-;SCHEMBL6929276;DTXSID20447377;AKOS005200800;2-(4-Methoxyphenylsulfonyl)-3-methylbutanoic acid

Suppliers and Price of Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl-

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 6 raw suppliers

Chemical Property of Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl-

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:272.07184478
Heavy Atom Count:18
Complexity:374

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)C(C(=O)O)S(=O)(=O)C1=CC=C(C=C1)OC

Technology Process of Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl-

There total 4 articles about Butanoic acid, 2-[(4-methoxyphenyl)sulfonyl]-3-methyl- 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: 96.0%

: 212769-90-9
2-(4-methoxybenzenesulfonyl)-3-methylbutyric acid ethyl ester

: 134649-63-1
2-(4-methoxybenzenesulfonyl)-3-methylbutyric acid

Guidance literature:: With sodium hydroxide; In methanol; at 20 ℃;
DOI:10.1021/jm0205548

Reference yield:

: 609-12-1
ethyl 2-bromoisovalerate

: 134649-63-1
2-(4-methoxybenzenesulfonyl)-3-methylbutyric acid

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / K₂CO₃ / acetone / 8 h / Heating

2: 99 percent / 3-chloroperoxybenzoic acid / CH₂Cl₂ / 20 °C

3: 96 percent / aq. NaOH / methanol / 20 °C

With sodium hydroxide; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; acetone;
DOI:10.1021/jm0205548

Reference yield:

: 696-63-9
4-Methoxybenzenethiol

: 134649-63-1
2-(4-methoxybenzenesulfonyl)-3-methylbutyric acid

Guidance literature:: Multi-step reaction with 3 steps

1: 99 percent / K₂CO₃ / acetone / 8 h / Heating

2: 99 percent / 3-chloroperoxybenzoic acid / CH₂Cl₂ / 20 °C

3: 96 percent / aq. NaOH / methanol / 20 °C

With sodium hydroxide; potassium carbonate; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; acetone;
DOI:10.1021/jm0205548