3-(1H-imidazol-5-yl)-2-oxopropanoic acid

Base Information

Chemical Name:3-(1H-imidazol-5-yl)-2-oxopropanoic acid
CAS No.:2504-83-8
Molecular Formula:C6H6 N2 O3
Molecular Weight:154.125
Hs Code.:2933290090
DSSTox Substance ID:DTXSID00274284
Nikkaji Number:J467.750A
Wikidata:Q72482313
Metabolomics Workbench ID:50902
Mol file:2504-83-8.mol

Synonyms:3-(1H-imidazol-5-yl)-2-oxopropanoic acid;2504-83-8;Imidazole pyruvate;3-(1H-imidazol-4-yl)-2-oxopropanoic acid;Imidazole pyruvic acid;imidazol-5-yl-pyruvate;3-(imidazol-5-yl)pyruvic acid;4-Imidazolylbrenztraubensaure;SCHEMBL1331769;3-(imidazol-4-yl)pyruvic acid;CHEBI:17406;CHEBI:59013;DTXSID00274284;AKOS006277771;3-(4-Imidazolyl)-2-oxopropionic acid;3-(1H-imidazol-4-yl)-2-oxopropanoicacid;C03277;EN300-1819553

Suppliers and Price of 3-(1H-imidazol-5-yl)-2-oxopropanoic 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

American Custom Chemicals Corporation
3-(4-IMIDAZOLYL)-2-OXOPROPIONIC ACID 98.00%
10G
$ 1824.90

Total 5 raw suppliers

Chemical Property of 3-(1H-imidazol-5-yl)-2-oxopropanoic acid

Chemical Property:

Boiling Point:466.2±28.0 °C(Predicted)
PKA:2.03±0.54(Predicted)
PSA：83.05000
Density:1.510±0.06 g/cm3(Predicted)
LogP:-0.39410
XLogP3:-0.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:154.03784206
Heavy Atom Count:11
Complexity:181

Purity/Quality:

98%Min ^*data from raw suppliers

3-(4-IMIDAZOLYL)-2-OXOPROPIONIC ACID 98.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=C(NC=N1)CC(=O)C(=O)O

Technology Process of 3-(1H-imidazol-5-yl)-2-oxopropanoic acid

There total 8 articles about 3-(1H-imidazol-5-yl)-2-oxopropanoic 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:

: 328-50-7
α-ketoglutaric acid

: 351-50-8
D-histidin

: 6893-26-1,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6
D-Glutamic acid

: 2504-83-8
β-imidazolyl pyruvic acid

Guidance literature:: With pyridoxal 5'-phosphate; recombinant Lactobacillus salivarius UCC₁₁₈ D-amino acid aminotransferase; In aq. phosphate buffer; at 30 ℃; for 0.0166667h; pH=7.5; Enzymatic reaction;
DOI:10.1016/j.molcatb.2013.04.013

Reference yield:

: 71-00-1
L-histidine

: 2504-83-8
β-imidazolyl pyruvic acid

Guidance literature:: With sodium hydroxide; hexacyanoferrate(III); at 35 ℃; Rate constant; Mechanism; Thermodynamic data; Ea; effect of concentration of reagents;