(2s)-Hydroxy(4-nitrophenyl)ethanoic acid

Base Information

Chemical Name:(2s)-Hydroxy(4-nitrophenyl)ethanoic acid
CAS No.:77977-72-1
Molecular Formula:C₈H₇NO₅
Molecular Weight:197.147
Hs Code.:
European Community (EC) Number:871-149-4
Nikkaji Number:J74.232E

Synonyms:(2s)-hydroxy(4-nitrophenyl)ethanoic acid;(2S)-2-hydroxy-2-(4-nitrophenyl)acetic acid;77977-72-1;(S)-2-Hydroxy-2-(4-nitrophenyl)acetic acid;SCHEMBL10170602;EN300-25915181

Suppliers and Price of (2s)-Hydroxy(4-nitrophenyl)ethanoic 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 15 raw suppliers

Chemical Property of (2s)-Hydroxy(4-nitrophenyl)ethanoic acid

Chemical Property:

XLogP3:0.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:197.03242232
Heavy Atom Count:14
Complexity:228

Purity/Quality:: 99% ,98%,Electron Grade , ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1C(C(=O)O)O)[N+](=O)[O-]
Isomeric SMILES:C1=CC(=CC=C1[C@@H](C(=O)O)O)[N+](=O)[O-]

Technology Process of (2s)-Hydroxy(4-nitrophenyl)ethanoic acid

There total 2 articles about (2s)-Hydroxy(4-nitrophenyl)ethanoic 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:

Reference yield:

: 62-76-0
sodium oxalate

: 555-16-8
4-nitrobenzaldehdye

: 77977-72-1
(S)-4-nitromandelic acid

: 77977-73-2
(R)-4-nitromandelic acid

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

Reference yield:

: 77977-72-1
(S)-4-nitromandelic acid

Guidance literature:

Reference yield:

: 77977-72-1
(S)-4-nitromandelic acid

: 13244-75-2
(S)-α,4-dihydroxy-benzeneacetic acid

Guidance literature:: Multi-step reaction with 3 steps

2: palladium/al3O₃; ethanol / Hydrogenation

3: Diazotization_.anschliessende Hydrolyse

With aluminum oxide; ethanol; palladium;