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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)-Methyl 2-amino-3-(5-methylpyridin-2-yl)propanoate hydrochloride

CN[C@H](C(=O)OC)Cc1ccccc1.Cl Request for Quotation
Chemical Name: (S)-Methyl 2-amino-3-(5-methylpyridin-2-yl)propanoate hydrochloride
CAS Number: 1810074-68-0
Product Number: AG0022LX(AGN-PC-0WAMAP)
Synonyms:
MDL No:
Molecular Formula: C11H16ClNO2
Molecular Weight: 229.7032

Identification/Properties

Computed Properties
Molecular Weight:
230.692g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
230.082g/mol
Monoisotopic Mass:
230.082g/mol
Topological Polar Surface Area:
65.2A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
197
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (S)-Methyl 2-amino-3-(5-methylpyridin-2-yl)propanoate hydrochloride is a valuable compound utilized in chemical synthesis for its role as a chiral building block. Its asymmetric nature makes it an essential component in the preparation of enantiomerically pure compounds, particularly in the pharmaceutical and agrochemical industries. This compound serves as a key intermediate in the synthesis of various bioactive molecules, providing a pathway for the creation of stereochemically defined products with enhanced biological activity. The (S)-Methyl 2-amino-3-(5-methylpyridin-2-yl)propanoate hydrochloride plays a crucial role in facilitating the development of new drugs and functional materials through strategic chemical transformations that capitalize on its stereochemical properties.