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(R)-4-NITROMANDELIC ACID

Base Information Edit
  • Chemical Name:(R)-4-NITROMANDELIC ACID
  • CAS No.:77977-73-2
  • Molecular Formula:C8H7NO5
  • Molecular Weight:197.14488
  • Hs Code.:2918199090
  • Mol file:77977-73-2.mol
(R)-4-NITROMANDELIC ACID

Synonyms:Benzeneaceticacid, a-hydroxy-4-nitro-, (R)-;(R)-(-)-p-Nitromandelic acid;(R)-4-Nitromandelic acid;( R)- 4-Nitromandelic Acid;hydroxy(4-nitrophenyl)acetic acid;benzeneacetic acid, α-hydroxy-4-nitro-;p-nitromandelic acid;4-nitrophenylglycolic acid;

Suppliers and Price of (R)-4-NITROMANDELIC ACID
Supply Marketing:Edit
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 (R)-4-NITROMANDELIC ACID Edit
Chemical Property:
  • Vapor Pressure:2.17E-08mmHg at 25°C 
  • Refractive Index:1.634 
  • Boiling Point:436.4 °C at 760 mmHg 
  • Flash Point:197.5 °C 
  • PSA:103.35000 
  • Density:1.552 g/cm3 
  • LogP:1.23600 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of (R)-4-NITROMANDELIC ACID

There total 3 articles about (R)-4-NITROMANDELIC 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 oxalyl Coenzyme A decarboxylase from Methylorubrum extorquens Y497A mutant; oxalyl Coenzyme A synthetase from from Methylorubrum extorquens; thioesterase YciA from Escherichia coli; thiamine diphosphate; ATP; coenzyme A; magnesium chloride; In dimethyl sulfoxide; at 30 ℃; for 24h; pH=6.8; enantioselective reaction; Enzymatic reaction;
DOI:10.1002/anie.201915155
Guidance literature:
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