Gemopatrilat metabolite M10

Base Information

Chemical Name:Gemopatrilat metabolite M10
CAS No.:84800-13-5
Molecular Formula:C₉H₁₀O₂S
Molecular Weight:182.243
Hs Code.:
UNII:A53XUF5CSX
Nikkaji Number:J938.592D
ChEMBL ID:CHEMBL82965

Synonyms:A53XUF5CSX;Gemopatrilat metabolite M10;Omapatrilat metabolite M1-b;UNII-A53XUF5CSX;BMS 196087;(2S)-3-phenyl-2-sulfanylpropanoic acid;Benzenepropanoic acid, alpha-mercapto-, (S)-;84800-13-5;Benzenepropanoic acid, alpha-mercapto-, (alphaS)-;1alw;CHEMBL82965;SCHEMBL4838500;BMS-196087;BENZENEPROPANOIC ACID, .ALPHA.-MERCAPTO-, (S)-;BENZENEPROPANOIC ACID, .ALPHA.-MERCAPTO-, (.ALPHA.S)-

Suppliers and Price of Gemopatrilat metabolite M10

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of Gemopatrilat metabolite M10

Chemical Property:

Vapor Pressure:0mmHg at 25°C
XLogP3:2.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:182.04015073
Heavy Atom Count:12
Complexity:153

Purity/Quality:

Safty Information:

Pictogram(s):
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MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(C(=O)O)S
Isomeric SMILES:C1=CC=C(C=C1)C[C@@H](C(=O)O)S

Technology Process of Gemopatrilat metabolite M10

There total 27 articles about Gemopatrilat metabolite M10 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: 96.9%