CAS 1365272-76-9: 2′-Cyano-N-ethyl[1,1′-biphenyl]-3-carboxamide

Description: 2′-Cyano-N-ethyl[1,1′-biphenyl]-3-carboxamide is a chemical compound characterized by its unique structural features, which include a cyano group, an ethyl amine moiety, and a carboxamide functional group attached to a biphenyl backbone. This compound typically exhibits moderate to high lipophilicity due to the biphenyl structure, which can influence its solubility and interaction with biological membranes. The presence of the cyano group may impart specific electronic properties, potentially affecting its reactivity and interactions in chemical processes. Additionally, the carboxamide group can participate in hydrogen bonding, enhancing its solubility in polar solvents. This compound may be of interest in various fields, including pharmaceuticals and materials science, due to its potential biological activity and utility in organic synthesis. As with many organic compounds, its stability, reactivity, and potential applications would depend on the specific conditions under which it is used, including temperature, pH, and the presence of other reactive species.

Formula: C₁₆H₁₄N₂O

InChI: InChI=1S/C16H14N2O/c1-2-18-16(19)13-8-5-7-12(10-13)15-9-4-3-6-14(15)11-17/h3-10H,2H2,1H3,(H,18,19)

InChI key: InChIKey=DDRYXNJIFJUPQE-UHFFFAOYSA-N

SMILES: N#CC=1C=CC=CC1C=2C=CC=C(C2)C(=O)NCC

[1,1'-Biphenyl]-3-carboxamide, 2'-cyano-N-ethyl-

CAS: 1365272-76-9

• Formula: C₁₆H₁₄N₂O
• Molecular weight: 250.2952

3-(2-Cyanophenyl)-N-ethylbenzamide

CAS: 1365272-76-9

• Purity: 98%
• Molecular weight: 250.30099487304688

3-(2-Cyanophenyl)-N-ethylbenzamide

CAS: 1365272-76-9

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• Formula: C₁₆H₁₄N₂O
• Purity: Min. 95%
• Molecular weight: 250.3 g/mol