gamma-Glutamyl-beta-cyanoalanine

Base Information

Chemical Name:gamma-Glutamyl-beta-cyanoalanine
CAS No.:16051-95-9
Molecular Formula:C₉H₁₃N₃O₅
Molecular Weight:243.219
Hs Code.:
UNII:SH78BZU8NN
DSSTox Substance ID:DTXSID60936331
Nikkaji Number:J640.876A
Wikidata:Q27108658
Metabolomics Workbench ID:71290
Mol file:16051-95-9.mol

Synonyms:gamma-Glutamyl-beta-cyanoalanine;3-Cyano-N-L-gamma-glutamyl-L-alanine;16051-95-9;L-Alanine, 3-cyano-N-L-gamma-glutamyl-;SH78BZU8NN;UNII-SH78BZU8NN;C05711;(2S)-2-amino-5-[[(1S)-1-carboxy-2-cyanoethyl]amino]-5-oxopentanoic acid;SCHEMBL1533819;CHEBI:10565;DTXSID60936331;N-(gamma-Glutamyl)-beta-cyanoalanine;AKOS037645634;AS-6191;L-Alanine, L-gamma-glutamyl-3-cyano-;N-[(1S)-1-carboxy-2-cyanoethyl]-L-glutamine;5-[(1-Carboxy-2-cyanoethyl)imino]-5-hydroxynorvaline;Q27108658;(2S)-2-amino-5-[[(1S)-1-carboxy-2-cyano-ethyl]amino]-5-oxo-pentanoic acid

Suppliers and Price of gamma-Glutamyl-beta-cyanoalanine

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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price

Total 0 raw suppliers

Chemical Property of gamma-Glutamyl-beta-cyanoalanine

Chemical Property:

PSA：157.00000
LogP:0.20218
XLogP3:-4.4
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:7
Exact Mass:243.08552052
Heavy Atom Count:17
Complexity:359

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CC(=O)NC(CC#N)C(=O)O)C(C(=O)O)N
Isomeric SMILES:C(CC(=O)N[C@@H](CC#N)C(=O)O)[C@@H](C(=O)O)N

Technology Process of gamma-Glutamyl-beta-cyanoalanine

There total 2 articles about gamma-Glutamyl-beta-cyanoalanine 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:

: (S)-2-((S)-4-Benzyloxycarbonyl-4-benzyloxycarbonylamino-butyrylamino)-3-cyano-propionic acid; compound with dicyclohexyl-amine

: 16051-95-9
N-(γ-L-Glutamyl)-β-cyano-L-alanine

Guidance literature:: Multistep reaction; (i) ion-exchange resin + form>, MeOH, (ii) H2, Pd;
DOI:10.1021/ja01038a058

Reference yield:

: 16051-95-9
N-(γ-L-Glutamyl)-β-cyano-L-alanine

Guidance literature:: β-Cyano-L-alanin, Carbobenzoxy-L-glutaminsaeure-α-benzylester, 1. Isobutylchlorcarbonat (gemischte Anhydrid Methode) (-> Carbobenzoxy-γ-L-glutamyl-β-cyano-L-alanin-α-benzylester), 2. Pd, Hydrogenolyse;
DOI:10.1021/ja00903a069