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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-, methyl ester, hydrochloride, (aS)-

COC(=O)[C@H](c1ccccc1)N Request for Quotation
Chemical Name: Benzeneacetic acid, a-amino-, methyl ester, hydrochloride, (aS)-
CAS Number: 15028-39-4
Product Number: AG00HXSA(AGN-PC-0Q4J46)
Synonyms:
MDL No: MFCD00077158
Molecular Formula:
Molecular Weight:

Identification/Properties

Computed Properties
Molecular Weight:
201.65g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
201.056g/mol
Monoisotopic Mass:
201.056g/mol
Topological Polar Surface Area:
52.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
153
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-Methyl 2-amino-2-phenylacetate hydrochloride, commonly known as $name$, is a versatile compound used in chemical synthesis procedures. This compound is renowned for its unique chiral structure, making it highly valuable in asymmetric synthesis. Asymmetric synthesis is a crucial technique in organic chemistry, allowing the production of enantiopure compounds with precise stereochemical control.In chemical synthesis, (S)-Methyl 2-amino-2-phenylacetate hydrochloride serves as a key building block for creating complex molecules with specific chirality. Its ability to selectively introduce chirality into molecules makes it a valuable tool in the pharmaceutical industry for producing optically pure drug compounds. By incorporating this compound into synthetic routes, chemists can efficiently access enantiomerically pure products with enhanced biological activity and reduced side effects.Furthermore, (S)-Methyl 2-amino-2-phenylacetate hydrochloride plays a crucial role in the synthesis of fine chemicals, agrochemicals, and materials with diverse applications. Its chiral nature allows for the creation of novel compounds with tailored properties and functionalities, making it a sought-after reagent in various research and development fields.Overall, the application of (S)-Methyl 2-amino-2-phenylacetate hydrochloride in chemical synthesis exemplifies its significance as a powerful tool for achieving stereochemical control and advancing the discovery of new molecules with important industrial and pharmaceutical applications.