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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-(acetylamino)-, (aR)-

OC(=O)[C@@H](c1ccccc1)NC(=O)C Request for Quotation
Chemical Name: Benzeneacetic acid, a-(acetylamino)-, (aR)-
CAS Number: 14257-84-2
Product Number: AG009GDJ(AGN-PC-0PSMQ6)
Synonyms:
MDL No:
Molecular Formula: C10H11NO3
Molecular Weight: 193.1992

Identification/Properties

Computed Properties
Molecular Weight:
193.202g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
193.074g/mol
Monoisotopic Mass:
193.074g/mol
Topological Polar Surface Area:
66.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
221
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


(R)-2-Acetamido-2-phenylacetic acid, a chiral compound, plays a crucial role as a versatile building block in chemical synthesis. With its specific stereochemistry, it is utilized in the construction of various pharmaceutical intermediates and fine chemicals. This compound serves as a key starting material in the synthesis of pharmaceuticals, agrochemicals, and other biologically active molecules, due to its ability to introduce specific functional groups with high stereochemical precision. Its application in asymmetric synthesis enables the creation of enantiomerically pure compounds, which are essential in the development of new drugs and materials. Furthermore, (R)-2-Acetamido-2-phenylacetic acid contributes to the advancement of organic chemistry by providing a platform for the creation of complex molecular structures with desired chirality, making it an indispensable tool for chemists in designing and producing valuable compounds.