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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-amino-4-fluoro-, (aS)-

N[C@@H](c1ccc(cc1)F)C(=O)O Request for Quotation
Chemical Name: Benzeneacetic acid, a-amino-4-fluoro-, (aS)-
CAS Number: 19883-57-9
Product Number: AG002BRM(AGN-PC-0QQ6FP)
Synonyms:
MDL No:
Molecular Formula: C8H8FNO2
Molecular Weight: 169.1530

Identification/Properties

Properties
MP:
≥300 °C
BP:
289.9°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Solubility:
Soluble in 1M HCl.
Computed Properties
Molecular Weight:
169.155g/mol
XLogP3:
-1.6
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
169.054g/mol
Monoisotopic Mass:
169.054g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
166
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:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-4-Fluorophenylglycine, a versatile compound frequently used in chemical synthesis, plays a crucial role in various reactions and processes within the field of chemistry. This chiral building block is particularly valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals due to its ability to impart specific stereochemical properties to synthesized compounds. Its application as a key intermediate in the synthesis of complex molecules allows for the creation of diverse structures with precise stereochemistry, making it a valuable tool for chemists working in the areas of drug discovery, materials science, and biotechnology. Additionally, (S)-4-Fluorophenylglycine serves as an essential component in the development of novel synthetic methodologies and strategies, enabling the rapid and efficient construction of molecular frameworks with desired properties. Its utilization in asymmetric synthesis and catalysis further enhances its utility in the creation of enantiomerically enriched compounds, thereby expanding the scope of chemical research and development. Whether employed in the design of new pharmaceutical agents or the synthesis of specialized materials, (S)-4-Fluorophenylglycine represents a fundamental building block with wide-ranging applications in chemical synthesis.