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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)-

(S)-2-Amino-3-(3-chlorophenyl)propanoic acid hydrochloride

OC(=O)[C@H](Cc1cccc(c1)Cl)N.Cl Request for Quotation
Chemical Name: (S)-2-Amino-3-(3-chlorophenyl)propanoic acid hydrochloride
CAS Number: 123053-22-5
Product Number: AG000K0K(AGN-PC-0WAMNC)
Synonyms:
MDL No:
Molecular Formula: C9H11Cl2NO2
Molecular Weight: 236.0951

Identification/Properties

Computed Properties
Molecular Weight:
236.092g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
235.017g/mol
Monoisotopic Mass:
235.017g/mol
Topological Polar Surface Area:
63.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
187
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-2-Amino-3-(3-chlorophenyl)propanoic acid hydrochloride is a valuable compound utilized in various chemical synthesis processes. This compound is commonly employed in the pharmaceutical industry as a key intermediate for the synthesis of important drugs and pharmaceuticals. Its asymmetric structure enables it to serve as a chiral building block in the production of enantiomerically pure compounds, which are crucial in drug development and manufacturing. Additionally, (S)-2-Amino-3-(3-chlorophenyl)propanoic acid hydrochloride is often used in the synthesis of peptides and other complex organic molecules due to its versatile chemical properties and reactivity. Its presence facilitates the formation of specific functional groups and stereochemistry necessary for the creation of novel chemical entities with potential therapeutic applications.