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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)-

L-Phenylalaninamide, N-[(phenylmethoxy)carbonyl]glycyl-

O=C(NCC(=O)N[C@H](C(=O)N)Cc1ccccc1)OCc1ccccc1 Request for Quotation
Chemical Name: L-Phenylalaninamide, N-[(phenylmethoxy)carbonyl]glycyl-
CAS Number: 5513-69-9
Product Number: AG00DCBL(AGN-PC-0OC6QT)
Synonyms:
MDL No:
Molecular Formula: C19H21N3O4
Molecular Weight: 355.3877

Identification/Properties

Computed Properties
Molecular Weight:
355.394g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
9
Exact Mass:
355.153g/mol
Monoisotopic Mass:
355.153g/mol
Topological Polar Surface Area:
111A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
471
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-Gly-Phe-NH2 is a key component in chemical synthesis, particularly in the field of peptide chemistry. This compound serves as a protected amino acid derivative, providing a versatile building block for the creation of complex peptides and peptide-like molecules. By incorporating Z-Gly-Phe-NH2 into peptide synthesis reactions, chemists can carefully control the selective deprotection of functional groups and ensure the desired coupling reactions occur with high yields and purity. Additionally, Z-Gly-Phe-NH2 plays a critical role in the protection of peptide bonds during the synthesis process, safeguarding sensitive intermediates and enabling the sequential assembly of longer peptide chains with precision and efficiency. Its strategic use in chemical synthesis empowers researchers to synthesize diverse peptides for applications in drug discovery, biological studies, and materials science.