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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)-

Benzeneacetic acid, a-[[(phenylmethoxy)carbonyl]amino]-

O=C(NC(c1ccccc1)C(=O)O)OCc1ccccc1 Request for Quotation
Chemical Name: Benzeneacetic acid, a-[[(phenylmethoxy)carbonyl]amino]-
CAS Number: 60584-76-1
Product Number: AG00F48U(AGN-PC-0SWRQE)
Synonyms:
MDL No:
Molecular Formula: C16H15NO4
Molecular Weight: 285.2946

Identification/Properties

Computed Properties
Molecular Weight:
285.299g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
6
Exact Mass:
285.1g/mol
Monoisotopic Mass:
285.1g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
346
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-(Benzyloxycarbonyl)-DL-phenylglycine, also known as Z-phenylglycine, is a versatile compound often utilized in chemical synthesis as a key building block for the production of various pharmaceuticals, peptides, and complex organic molecules. This compound serves as a crucial intermediate in the synthesis of peptide derivatives, allowing for the selective protection of the amino group and subsequent manipulation of the carboxylic acid functionality. Its unique chemical properties enable precise control over the reactivity and selectivity of the amino and carboxylic acid groups, facilitating the synthesis of structurally diverse and biologically active compounds. In addition, N-(Benzyloxycarbonyl)-DL-phenylglycine plays a vital role in the development of new drug candidates and the study of peptide chemistry, making it an invaluable tool for researchers and chemists in the field of organic synthesis.