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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)-

(R)-2-Amino-1-(pyridin-3-yl)ethanol hydrochloride

NC[C@@H](c1cccnc1)O.Cl Request for Quotation
Chemical Name: (R)-2-Amino-1-(pyridin-3-yl)ethanol hydrochloride
CAS Number: 1038594-01-2
Product Number: AG007FEQ(AGN-PC-0WA2JM)
Synonyms:
MDL No:
Molecular Formula: C7H11ClN2O
Molecular Weight: 174.6280

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The (R)-2-Amino-1-(pyridin-3-yl)ethanol hydrochloride is a valuable compound commonly utilized in chemical synthesis due to its versatile reactivity and unique structural features. This compound serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its chiral nature, stemming from the presence of the amino and alcohol functional groups, enables precise control over stereochemistry in synthetic pathways. Furthermore, the pyridine moiety enhances the compound's reactivity in cross-coupling reactions and serves as a directing group in complex organic transformations. The (R)-2-Amino-1-(pyridin-3-yl)ethanol hydrochloride plays a crucial role in the creation of intricate molecular architectures and the development of novel chemical entities with diverse applications.