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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)-

Z-Ala-Gly-OH

C[C@@H](C(=O)NCC(=O)O)NC(=O)OCc1ccccc1 Request for Quotation
Chemical Name: Z-Ala-Gly-OH
CAS Number: 3235-17-4
Product Number: AG00C7SU(AGN-PC-0WBO2Y)
Synonyms:
MDL No:
Molecular Formula: C13H16N2O5
Molecular Weight: 280.2765

Identification/Properties

Properties
Storage:
Room Temperature;
Computed Properties
Molecular Weight:
280.28g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
7
Exact Mass:
280.106g/mol
Monoisotopic Mass:
280.106g/mol
Topological Polar Surface Area:
105A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
353
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


Z-Ala-Gly-OH, a dipeptide consisting of the amino acids alanine and glycine linked together, is a valuable tool in chemical synthesis. This compound is commonly used as a building block in peptide synthesis to create more complex peptides or proteins. It serves as a key intermediate in the formation of longer peptide chains by enabling the controlled addition of amino acids in a specific sequence. Z-Ala-Gly-OH plays a crucial role in solid-phase peptide synthesis, where it can be attached to a solid support and sequentially elongated to construct custom peptides with precise sequences. Additionally, Z-Ala-Gly-OH can be utilized in the pharmaceutical industry for the development of peptide-based drugs or as a research tool in biochemistry studies. Its versatility and compatibility with various synthetic methods make Z-Ala-Gly-OH a fundamental component in the realm of chemical synthesis.