CAS 94441-89-1

N-[(1S)-3-Methyl-1-[(2-naphthalenylamino)carbonyl]butyl]benzamide

Description:

N-[(1S)-3-Methyl-1-[(2-naphthalenylamino)carbonyl]butyl]benzamide, with the CAS number 94441-89-1, is a chemical compound characterized by its complex structure, which includes a benzamide moiety and a naphthalenyl group. This compound features a chiral center, indicated by the (1S) configuration, which can influence its biological activity and interactions. The presence of the naphthalenyl group suggests potential aromatic interactions, while the carbonyl and amine functionalities may contribute to hydrogen bonding capabilities. Such structural characteristics often imply that the compound could exhibit specific pharmacological properties, making it of interest in medicinal chemistry. Additionally, the compound's solubility, stability, and reactivity would depend on its molecular interactions and the surrounding environment. As with many organic compounds, its behavior in biological systems would be influenced by factors such as pH, temperature, and the presence of other molecules. Overall, this compound's unique structure positions it as a candidate for further research in various chemical and pharmaceutical applications.

Formula: C₂₃H₂₄N₂O₂

InChI: InChI=1S/C23H24N2O2/c1-16(2)14-21(25-22(26)18-9-4-3-5-10-18)23(27)24-20-13-12-17-8-6-7-11-19(17)15-20/h3-13,15-16,21H,14H2,1-2H3,(H,24,27)(H,25,26)/t21-/m0/s1

InChI key: InChIKey=QTJKADZPYFJSEQ-NRFANRHFSA-N

SMILES: N(C([C@@H](NC(=O)C1=CC=CC=C1)CC(C)C)=O)C2=CC3=C(C=C2)C=CC=C3

Synonyms:

• (S)-N-Benzoyl-leucine β-naphthylamide
• Benzamide, N-[(1S)-3-methyl-1-[(2-naphthalenylamino)carbonyl]butyl]-
• Benzamide, N-[3-methyl-1-[(2-naphthalenylamino)carbonyl]butyl]-, (S)-
• N-[(1S)-3-Methyl-1-[(2-naphthalenylamino)carbonyl]butyl]benzamide
• N-naphthalen-2-yl-N~2~-(phenylcarbonyl)leucinamide
• (S)-N-(3-Methyl-1-((2-naphthylamino)carbonyl)butyl)benzamide

N-Benzoyl-L-leucine-beta-naphthylamide

CAS: 94441-89-1

N-Benzoyl-L-leucine-beta-naphthylamide is a chromogenic substrate for transpeptidase. It is hydrolyzed to L-phenylalanine and 2-naphthylamine, which react with the chromogen to produce a color change. The reaction occurs in both spermatozoa and epithelial cells, but can be inhibited by aminopeptidase and peptidase. This substrate is used as a marker for spermatozoa in semen analysis.

Formula: C₂₃H₂₄N₂O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 360.45 g/mol

Ref: 3D-FB65756