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CAS 37440-01-0

:

(αR)-α-(Acetylamino)-2-naphthalenepropanoic acid

Description:
(αR)-α-(Acetylamino)-2-naphthalenepropanoic acid, also known by its CAS number 37440-01-0, is a chemical compound characterized by its unique structural features, which include a naphthalene ring system and an acetylamino group. This compound typically exhibits properties associated with both aromatic and aliphatic functionalities, contributing to its potential biological activity. It is a chiral molecule, meaning it has non-superimposable mirror images, which can influence its interaction with biological systems, particularly in pharmacology. The presence of the acetylamino group suggests that it may participate in hydrogen bonding, affecting its solubility and reactivity. Additionally, the naphthalene moiety can provide hydrophobic characteristics, which may influence its distribution in biological environments. Overall, this compound may be of interest in medicinal chemistry and drug development due to its structural complexity and potential therapeutic applications. However, specific physical and chemical properties such as melting point, solubility, and spectral data would require further investigation or reference to specialized databases for precise information.
Formula:C15H15NO3
InChI:InChI=1S/C15H15NO3/c1-10(17)16-14(15(18)19)9-11-6-7-12-4-2-3-5-13(12)8-11/h2-8,14H,9H2,1H3,(H,16,17)(H,18,19)/t14-/m1/s1
InChI key:InChIKey=HGTIILKZSFKZMS-CQSZACIVSA-N
SMILES:C([C@@H](NC(C)=O)C(O)=O)C1=CC2=C(C=C1)C=CC=C2
Synonyms:
  • (2R)-2-(acetylamino)-3-naphthalen-2-ylpropanoate
  • (2R)-2-Acetamido-3-naphthalen-2-ylpropanoic acid
  • (R)-2-Acetamido-3-(naphthalen-2-yl)propanoicacid
  • (R)-2-Acetylamino-3-(2-naphthyl)propanoic acid
  • (r)-2-Acetamido-3-(naphthalen-2-yl)propanoic acid
  • (αR)-α-(Acetylamino)-2-naphthalenepropanoic acid
  • 2-Naphthalenepropanoic acid, α-(acetylamino)-, (R)-
  • 2-Naphthalenepropanoic acid, α-(acetylamino)-, (αR)-
  • Ac-D-2-Nal-OH
  • N-Acetyl-D-2-naphthylalanine
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