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CAS 177839-86-0

:

Benzenebutanoic acid, β-amino-4-methoxy-, (R)-

Description:
Benzenebutanoic acid, β-amino-4-methoxy-, (R)-, with the CAS number 177839-86-0, is a chiral compound characterized by its specific stereochemistry, which is indicated by the (R) designation. This compound features a benzenebutanoic acid backbone, incorporating a β-amino group and a methoxy substituent at the para position of the benzene ring. The presence of the amino group contributes to its potential as a biological active molecule, possibly influencing its interaction with biological systems. The methoxy group enhances the lipophilicity of the compound, which can affect its solubility and permeability. As a carboxylic acid, it exhibits acidic properties, allowing it to participate in various chemical reactions, including esterification and amidation. The stereochemistry of the compound may also play a crucial role in its pharmacological activity, as different enantiomers can exhibit significantly different biological effects. Overall, this compound's unique structure and functional groups make it of interest in medicinal chemistry and related fields.
Formula:C11H15NO3
InChI:InChI=1S/C11H15NO3/c1-15-10-4-2-8(3-5-10)6-9(12)7-11(13)14/h2-5,9H,6-7,12H2,1H3,(H,13,14)/t9-/m1/s1
InChI key:InChIKey=GQFFGGKZIKRIFE-SECBINFHSA-N
SMILES:C([C@H](CC(O)=O)N)C1=CC=C(OC)C=C1
Synonyms:
  • (3R)-3-Amino-4-(4-methoxyphenyl)butanoic acid
  • Benzenebutanoic acid, β-amino-4-methoxy-, (R)-
  • benzenebutanoic acid, beta-amino-4-methoxy-, (betaR)-
  • (R)-3-Amino-4-(4-methoxyphenyl)butanoic acid
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