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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-[(4-methylphenyl)sulfonyl]-

OC(=O)[C@H](NS(=O)(=O)c1ccc(cc1)C)Cc1ccccc1 Request for Quotation
Chemical Name: D-Phenylalanine, N-[(4-methylphenyl)sulfonyl]-
CAS Number: 86117-53-5
Product Number: AG00IDWX(AGN-PC-0OK588)
Synonyms:
MDL No:
Molecular Formula: C16H17NO4S
Molecular Weight: 319.3755

Identification/Properties

Computed Properties
Molecular Weight:
319.375g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
6
Exact Mass:
319.088g/mol
Monoisotopic Mass:
319.088g/mol
Topological Polar Surface Area:
91.8A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
457
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-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-2-(4-Methylphenylsulfonamido)-3-phenylpropanoic acid, also known as $name$, serves as a valuable component in chemical synthesis as a chiral building block. This compound offers a versatile platform for creating various pharmaceuticals, agrochemicals, and materials with enhanced stereochemical purity. Its asymmetric center enables precise control over the stereochemistry of the final product, making it a crucial tool in the synthesis of enantiopure compounds. By incorporating $name$ into synthetic routes, chemists can access a diverse range of structurally complex molecules with specific stereochemical characteristics, thereby opening up new possibilities for drug discovery, material science, and other fields requiring highly pure chiral compounds.