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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Glycine, L-g-glutamyl-L-cysteinyl-, diethyl ester

CCOC(=O)CNC(=O)[C@@H](NC(=O)CC[C@@H](C(=O)OCC)N)CS Request for Quotation
Chemical Name: Glycine, L-g-glutamyl-L-cysteinyl-, diethyl ester
CAS Number: 97451-40-6
Product Number: AG00IJY4(AGN-PC-0W7501)
Synonyms:
MDL No:
Molecular Formula: C14H25N3O6S
Molecular Weight: 363.4298

Identification/Properties

Computed Properties
Molecular Weight:
363.429g/mol
XLogP3:
-0.8
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
13
Exact Mass:
363.146g/mol
Monoisotopic Mass:
363.146g/mol
Topological Polar Surface Area:
138A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
446
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (S)-Ethyl 2-amino-5-(((R)-1-((2-ethoxy-2-oxoethyl)amino)-3-mercapto-1-oxopropan-2-yl)amino)-5-oxopentanoate in chemical synthesis primarily lies in its role as a versatile building block for the construction of complex peptide structures. Its unique structure containing multiple functional groups allows for selective reactions and diverse manipulations in peptide synthesis. By incorporating (S)-Ethyl 2-amino-5-(((R)-1-((2-ethoxy-2-oxoethyl)amino)-3-mercapto-1-oxopropan-2-yl)amino)-5-oxopentanoate into peptide chains, chemists can enhance stereochemical control, introduce specific functional groups, and facilitate the formation of intricate peptide architectures for various pharmaceutical or biotechnological applications.