Lcj4RS3nle

Base Information

Chemical Name:Lcj4RS3nle
CAS No.:145679-14-7
Molecular Formula:C₁₀H₁₀O₄
Molecular Weight:194.187
Hs Code.:
UNII:LCJ4RS3NLE
Nikkaji Number:J608.399D

Synonyms:LCJ4RS3NLE;UNII-LCJ4RS3NLE;145679-14-7;4-((1S)-2-Hydroxy-1-methyl-2-oxo-ethyl)benzoic acid;Benzeneacetic acid, 4-carboxy-alpha-methyl-, (S)-;SCHEMBL6688306;BENZENEACETIC ACID, 4-CARBOXY-.ALPHA.-METHYL-, (S)-

Suppliers and Price of Lcj4RS3nle

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
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Total 0 raw suppliers

Chemical Property of Lcj4RS3nle

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:194.05790880
Heavy Atom Count:14
Complexity:228

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of Lcj4RS3nle

There total 1 articles about Lcj4RS3nle 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:

: 201230-82-2
carbon monoxide

: 1075-49-6
4-ethenylbenzoic acid

: 145679-14-7
para-(1-carboxy-ethyl)benzoic acid

: 145679-19-2
para-(1-carboxy-ethyl)benzoic acid

Guidance literature:: With ((R)-(-)-4,12-bis(bis(3,5-trifluoromethylphenyl)phosphino)-[2,2]-paracyclophane)dipalladium tetrachloride; toluene-4-sulfonic acid; lithium chloride; In water; butanone; at 50 ℃; for 22h; under 22502.3 Torr; Overall yield = 91 %Spectr.; enantioselective reaction; Inert atmosphere; Autoclave;
DOI:10.1039/c3cc41291a