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CAS 148278-94-8

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(2S)-2-amino-3-methoxypropan-1-ol

Description:
(2S)-2-amino-3-methoxypropan-1-ol, also known as a chiral amino alcohol, is characterized by its specific stereochemistry, indicated by the (2S) designation, which refers to the configuration around the second carbon atom in the chain. This compound features an amino group (-NH2) and a methoxy group (-OCH3) attached to a three-carbon backbone, contributing to its potential as a building block in organic synthesis and pharmaceutical applications. The presence of both an amino and an alcohol functional group allows for diverse reactivity, including the formation of amides and esters. Its solubility in polar solvents, such as water and alcohols, is notable due to the ability of the hydroxyl and amino groups to engage in hydrogen bonding. Additionally, the compound's chirality may influence its biological activity, making it relevant in the development of enantiomerically pure drugs. Overall, (2S)-2-amino-3-methoxypropan-1-ol is a versatile compound with significant implications in medicinal chemistry and synthetic organic chemistry.
Formula:C4H12ClNO2
InChI:InChI=1/C4H11NO2/c1-7-3-4(5)2-6/h4,6H,2-3,5H2,1H3/t4-/m0/s1
SMILES:COC[C@H](CO)N
Synonyms:
  • (S)-2-Amino-3-methoxy-1-propanol
  • 1-propanol, 2-amino-3-methoxy-, (2S)-
  • (2S)-2-Amino-3-methoxypropan-1-ol
  • 1-Propanol, 2-amino-3-methoxy-, hydrochloride, (2S)- (9CI)
  • (S)-2-amino-3-methoxypropan-1-ol hydrochloride
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