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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)-

BOC-(S)-3-AMINO-3-(3-FLUORO-PHENYL)-PROPIONIC ACID

OC(=O)C[C@@H](c1cccc(c1)F)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: BOC-(S)-3-AMINO-3-(3-FLUORO-PHENYL)-PROPIONIC ACID
CAS Number: 500770-72-9
Product Number: AG00DE0R(AGN-PC-0OB64T)
Synonyms:
MDL No:
Molecular Formula: C14H18FNO4
Molecular Weight: 283.2954

Identification/Properties

Computed Properties
Molecular Weight:
283.299g/mol
XLogP3:
2.1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
283.122g/mol
Monoisotopic Mass:
283.122g/mol
Topological Polar Surface Area:
75.6A^2
Heavy Atom Count:
20
Formal Charge:
0
Complexity:
354
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:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-3-((tert-Butoxycarbonyl)amino)-3-(3-fluorophenyl)propanoic acid is utilized as a key building block in chemical synthesis processes. It functions as a chiral auxiliary in asymmetric synthesis, enabling the production of enantiopure compounds with high selectivity. Its unique structural properties play a crucial role in controlling the stereochemistry of reactions, leading to the formation of complex molecules with precise stereochemical configurations. This compound is particularly valuable in the pharmaceutical industry for the preparation of chiral drug molecules and in the research field for the development of novel materials with specific functionalities.