(S)-1-(2-Aminopyridin-3-yl)ethanol|936718-00-2,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

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)-1-(2-Aminopyridin-3-yl)ethanol

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Chemical Name:	(S)-1-(2-Aminopyridin-3-yl)ethanol
CAS Number:	936718-00-2
Product Number:	AG0061LT(AGN-PC-0WAIE5)
Synonyms:
MDL No:
Molecular Formula:	C7H10N2O
Molecular Weight:	138.1671

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Keep in dry area;2-8℃;

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Chemical Structure

(S)-1-(2-Aminopyridin-3-yl)ethanol, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. In organic chemistry, it serves as a key intermediate in the formation of various compounds with valuable pharmacological and industrial applications. This compound can be utilized as a chiral starting material due to its specific stereochemistry, allowing for the synthesis of enantiomerically pure molecules. Furthermore, (S)-1-(2-Aminopyridin-3-yl)ethanol can be employed in the development of pharmaceuticals, agrochemicals, and functional materials, showcasing its significance in the field of synthetic chemistry. Its unique structural properties make it a valuable tool for creating complex molecular architectures with tailored properties, making it a valuable asset in the realm of chemical synthesis.