CAS 93779-34-1

(αR)-α-Amino-2-naphthaleneacetic acid

Description:

(αR)-α-Amino-2-naphthaleneacetic acid, commonly referred to as a naphthalene derivative, is an amino acid characterized by its naphthalene ring structure, which contributes to its unique properties. This compound features an amino group (-NH2) and a carboxylic acid group (-COOH), making it an α-amino acid. Its stereochemistry is defined by the (αR) configuration, indicating the specific spatial arrangement of its atoms. This compound is often studied for its potential biological activities, including interactions with various receptors and enzymes. It may exhibit properties such as solubility in polar solvents, and its naphthalene moiety can influence its hydrophobic interactions. The presence of the amino and carboxylic acid functional groups allows for participation in hydrogen bonding and ionic interactions, which are crucial for its biological function. Overall, (αR)-α-Amino-2-naphthaleneacetic acid serves as a valuable compound in biochemical research and may have implications in drug design and development.

Formula: C₁₂H₁₁NO₂

InChI: InChI=1S/C12H11NO2/c13-11(12(14)15)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H,13H2,(H,14,15)/t11-/m1/s1

InChI key: InChIKey=XAJPMFUAJFQIIT-LLVKDONJSA-N

SMILES: [C@@H](C(O)=O)(N)C1=CC2=C(C=C1)C=CC=C2

Synonyms:

• 2-Naphthaleneacetic acid, α-amino-, (αR)-
• (R)-Amino-naphthalen-2-yl-acetic acid
• (R)-2-Amino-2-(naphthalen-2-yl)acetic acid
• (αR)-α-Amino-2-naphthaleneacetic acid
• 2-Naphthaleneacetic acid, α-amino-, (R)-