Glutamyl-Valine

Base Information

Chemical Name:Glutamyl-Valine
CAS No.:5879-06-1
Molecular Formula:C₁₀H₁₈N₂O₅
Molecular Weight:246.263
Hs Code.:
DSSTox Substance ID:DTXSID60974314
Nikkaji Number:J785.310F
Wikidata:Q27137211
Metabolomics Workbench ID:78795
Mol file:5879-06-1.mol

Synonyms:H-GLU-VAL-OH;GLU-VAL;Glutamylvaline;Glutamyl-Valine;L-Glu-L-Val;alpha-Glu-Val;5879-06-1;L-Glutamyl-L-valine;(4S)-4-amino-5-[[(1S)-1-carboxy-2-methylpropyl]amino]-5-oxopentanoic acid;EV dipeptide;E-V Dipeptide;(4S)-4-amino-5-{[(1S)-1-carboxy-2-methylpropyl]amino}-5-oxopentanoic acid;L-alpha-Glu-L-Val;Glutamate Valine dipeptide;Glutamate-Valine dipeptide;L-alpha-glutamyl-L-valine;SCHEMBL537127;CHEBI:68846;DTXSID60974314;SITLTJHOQZFJGG-XPUUQOCRSA-N;HY-P4226;MFCD00037306;CS-0653214;Q27137211;(S)-4-amino-5-((S)-1-carboxy-2-methylpropylamino)-5-oxopentanoic acid

Suppliers and Price of Glutamyl-Valine

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
GLU-VAL 98.00%
1G
$ 1149.23

Total 10 raw suppliers

Chemical Property of Glutamyl-Valine

Chemical Property:

Vapor Pressure:1.41E-13mmHg at 25°C
Boiling Point:550.7°Cat760mmHg
Flash Point:286.8°C
PSA：129.72000
Density:1.272g/cm³
LogP:0.49510
Storage Temp.:-15°C
XLogP3:-3.9
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:7
Exact Mass:246.12157168
Heavy Atom Count:17
Complexity:303

Purity/Quality:

99% ^*data from raw suppliers

GLU-VAL 98.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Glutamyl-Valine

There total 10 articles about Glutamyl-Valine 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:

: 85701-66-2
N-(N-benzyloxycarbonyl-L-α-glutamyl)-L-valine

: 5879-06-1
L-glutamyl-L-valine

Guidance literature:: With methanol; palladium; Hydrogenation;
DOI:10.1039/jr9500001954

Reference yield:

: 4579-28-6
N-Benzyloxycarbonyl-α-L-glutamyl-L-valin-methylester

: 5879-06-1
L-glutamyl-L-valine

Guidance literature:: Multi-step reaction with 2 steps

1: aq. NaOH / Ambient temperature

2: H₂ / Pd-C / methanol; H₂O / 1520 Torr

With sodium hydroxide; hydrogen; palladium on activated charcoal; In methanol; water;
DOI:10.1021/jo01037a043

Reference yield:

: 6306-52-1
L-valine methylester hydrochloride

: 5879-06-1
L-glutamyl-L-valine

Guidance literature:: Multi-step reaction with 4 steps

1: (i) 2-ethyl-5-(3-sulfo-phenyl)-isoxazolium betaine, Et₃N, MeCN, (ii) /BRN= 3594960/, Et₃N

2: MnO₂, aq. AcOH / Ambient temperature

3: aq. NaOH / Ambient temperature

4: H₂ / Pd-C / methanol; H₂O / 1520 Torr

With manganese(IV) oxide; sodium hydroxide; hydrogen; acetic acid; palladium on activated charcoal; In methanol; water;
DOI:10.1021/jo01037a043