Benzyl 3-oxo-2-(phenylsulfanyl)butanoate

Base Information

Chemical Name:Benzyl 3-oxo-2-(phenylsulfanyl)butanoate
CAS No.:139101-20-5
Molecular Formula:C₁₇H₁₆O₃S
Molecular Weight:300.378
Hs Code.:
DSSTox Substance ID:DTXSID30576849
Nikkaji Number:J462.347I

Synonyms:139101-20-5;Benzyl 3-oxo-2-(phenylsulfanyl)butanoate;DTXSID30576849

Suppliers and Price of Benzyl 3-oxo-2-(phenylsulfanyl)butanoate

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 1 raw suppliers

Chemical Property of Benzyl 3-oxo-2-(phenylsulfanyl)butanoate

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:300.08201554
Heavy Atom Count:21
Complexity:344

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C(C(=O)OCC1=CC=CC=C1)SC2=CC=CC=C2

Technology Process of Benzyl 3-oxo-2-(phenylsulfanyl)butanoate

There total 1 articles about Benzyl 3-oxo-2-(phenylsulfanyl)butanoate 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:

: 5396-89-4
benzyl acetoacetate

: 931-59-9
benzenesulfenyl chloride

: 139101-20-5
benzyl 2-(phenylthio)-3-oxobutyrate

Guidance literature:: With sodium hydride; In tetrahydrofuran; Yield given;
DOI:10.1021/jo00033a058

Reference yield:

: 139101-20-5
benzyl 2-(phenylthio)-3-oxobutyrate

: 139101-26-1
benzyl 2-fluoro-2-(phenylthio)-3-oxobutyrate

Guidance literature:: With perchloryl fluoride; sodium hydride; Yield given. Multistep reaction; 1.) MeOH, 2.) THF, 0 deg C, 1.5 h;
DOI:10.1021/jo00033a058