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4-BROMOMANDELIC ACID

Base Information
  • Chemical Name:4-BROMOMANDELIC ACID
  • CAS No.:7021-04-7
  • Molecular Formula:C8H7BrO3
  • Molecular Weight:231.04300
  • Hs Code.:
  • Mol file:7021-04-7.mol
4-BROMOMANDELIC ACID

Synonyms:(R)-p-bromo-mandelic acid;(-)-4-Bromomandelic acid;p-Bromomandelic acid,(-);Benzeneacetic acid, 4-bromo-α-hydroxy-, (±)-;4-Brom-(R)-(-)-mandelsaeure;(R)-(-)-4-bromomandelic acid;D-4-bromomandelic acid;(R)-4-Brom-mandelsaeure;

Suppliers and Price of 4-BROMOMANDELIC ACID
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 16 raw suppliers
Chemical Property of 4-BROMOMANDELIC ACID
Chemical Property:
  • Melting Point:116-118oC(lit.) 
  • Refractive Index:1.4730 (estimate) 
  • PSA:57.53000 
  • Density:1.6494 (rough estimate) 
  • LogP:1.56710 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s): Xi 
  • Hazard Codes:Xi 
  • Statements: 36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of 4-BROMOMANDELIC ACID

There total 11 articles about 4-BROMOMANDELIC ACID 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:
Guidance literature:
With fluoroacetate dehalogenase RPA1163-W185T; for 1h; enantioselective reaction; Catalytic behavior; Kinetics; Enzymatic reaction;
DOI:10.1021/acscatal.9b04804
Guidance literature:
In acetonitrile; at 80 ℃; for 1.5h; Overall yield = 0.380 g; enantiospecific reaction; Resolution of racemate;
DOI:10.3390/molecules26185536
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