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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-Phenylalanine, 2,6-difluoro-

N[C@H](C(=O)O)Cc1c(F)cccc1F Request for Quotation
Chemical Name: L-Phenylalanine, 2,6-difluoro-
CAS Number: 33787-05-2
Product Number: AG00BYTO(AGN-PC-0O92N7)
Synonyms:
MDL No:
Molecular Formula: C9H9F2NO2
Molecular Weight: 201.1701

Identification/Properties

Computed Properties
Molecular Weight:
201.173g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
3
Exact Mass:
201.06g/mol
Monoisotopic Mass:
201.06g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
203
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


The (S)-2-Amino-3-(2,6-difluorophenyl)propanoic acid, also known as $name$, is a versatile compound commonly used in chemical synthesis. Its primary application lies in its role as a chiral building block in the production of pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, (S)-2-Amino-3-(2,6-difluorophenyl)propanoic acid serves as a crucial starting material for the creation of enantiomerically pure compounds. Its chiral nature allows for the controlled production of single enantiomers, which is essential for many industries that require high levels of purity and specificity in their chemical products.Furthermore, this compound can be utilized in the synthesis of complex molecules and drug candidates where stereochemistry plays a critical role in their biological activity and effectiveness. By incorporating (S)-2-Amino-3-(2,6-difluorophenyl)propanoic acid into synthetic pathways, chemists can access a wide range of chirally pure substances with precise control over their stereochemical properties.Overall, (S)-2-Amino-3-(2,6-difluorophenyl)propanoic acid is a valuable tool in chemical synthesis, enabling the creation of sophisticated molecules with enhanced stereochemical control and potential applications in various industries.