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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)-

D-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-, methyl ester

COC(=O)[C@@H](Cc1ccccc1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: D-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-, methyl ester
CAS Number: 77119-84-7
Product Number: AG005EEQ(AGN-PC-0OHY1F)
Synonyms:
MDL No:
Molecular Formula: C15H21NO4
Molecular Weight: 279.3315

Identification/Properties

Properties
BP:
403.7±38.0°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
279.336g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
7
Exact Mass:
279.147g/mol
Monoisotopic Mass:
279.147g/mol
Topological Polar Surface Area:
64.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
329
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, (R)-Methyl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate plays a crucial role as a versatile building block. It can be utilized as a chiral synthon in the preparation of various pharmaceutical intermediates and complex organic molecules. Its unique stereochemical properties make it valuable for the asymmetric synthesis of biologically active compounds. Additionally, (R)-Methyl 2-((tert-butoxycarbonyl)amino)-3-phenylpropanoate can be employed in the construction of peptide derivatives and other structurally diverse organic compounds, making it an essential component in modern chemical research and development.