CAS 3278-14-6
:N-(2-phenylethyl)benzamide
Description:
N-(2-phenylethyl)benzamide, with the CAS number 3278-14-6, is an organic compound characterized by its amide functional group and aromatic structure. It features a benzamide core, where a phenylethyl group is attached to the nitrogen atom of the amide. This compound typically appears as a white to off-white solid and is soluble in organic solvents such as ethanol and dichloromethane, but has limited solubility in water due to its hydrophobic aromatic components. The presence of both the phenyl and ethyl groups contributes to its potential applications in pharmaceuticals and organic synthesis, as these groups can influence the compound's biological activity and reactivity. N-(2-phenylethyl)benzamide may exhibit various chemical properties, including the ability to participate in hydrogen bonding due to the amide group, which can affect its melting point and boiling point. Overall, this compound is of interest in medicinal chemistry and material science for its structural characteristics and potential functional applications.
Formula:C15H15NO
InChI:InChI=1S/C15H15NO/c17-15(14-9-5-2-6-10-14)16-12-11-13-7-3-1-4-8-13/h1-10H,11-12H2,(H,16,17)
InChI key:InChIKey=DAVRGGJTJDTVQT-UHFFFAOYSA-N
SMILES:C(NCCC1=CC=CC=C1)(=O)C2=CC=CC=C2
Synonyms:- Benzamide, N-(2-phenylethyl)-
- Benzamide, N-phenethyl-
- Benzeneethanamine, N-benzoyl-
- N-(2-Phenylethyl)benzamid
- N-(2-Phenylethyl)benzolcarboxamid
- N-Benzoyl-2-phenylethylamine
- N-Benzoyl-β-phenethylamine
- N-Benzoylphenethylamine
- N-Phenethylbenzamide
- N-benzoyl-beta-phenylethylamine
- NSC 16618
- NSC 43723
- Riparin A
- N-(2-Phenylethyl)benzamide
- Solina New Impurity 21
- N-phenyl benzamide impurity
- N-phenethylbenzamide (solina new impurity)
- Solifenacin Related Compound 21 (N-Phenethylbenzamide)
- 4-(DICHLOROMETHYL)PYRIDINE HCL
- See more synonyms
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Found 10 products.
Solifenacin Impurity 29
CAS:Formula:C15H15NOColor and Shape:White To Off-White SolidMolecular weight:225.29N-phenethylbenzamide
CAS:<p>N-phenethylbenzamide (Solina New Impurity 21) is a natural product.</p>Formula:C15H15NOPurity:99.5%Color and Shape:SolidMolecular weight:225.29N-Phenethylbenzamide
CAS:Controlled Product<p>Applications N-Phenethylbenzamide was used for the synthesis of deteurerium-labeled amides within microreactors.<br>References Hooper, J., Watts, P.: J. Labelled Compd. Rad., 50, 189 (2007)<br></p>Formula:C15H15NOColor and Shape:NeatMolecular weight:225.29N-(2-Phenethyl)benzamide
CAS:<p>N-(2-Phenethyl)benzamide (NPEB) is a molecule that belongs to the group of reactive molecules. It has been shown to be toxic to gram-positive bacteria, such as Staphylococcus aureus and Bacillus subtilis, but not gram-negative bacteria such as Escherichia coli. NPEB also has been shown to have locomotor activity in animals, which may be due to its ability to inhibit the mitochondrial electron transport chain and inhibit ATP production. NPEB's biological properties are well characterized. FTIR spectroscopy showed that this molecule has an amide functional group and is a small molecule with a molecular weight of 176.4 g/mol. This molecule was also found to be able to bind to mitochondria in animals.</p>Formula:C15H15NOPurity:Min. 97 Area-%Color and Shape:PowderMolecular weight:225.29 g/molN-Phenethylbenzamide
CAS:Formula:C15H15NOPurity:95%Color and Shape:No data available.Molecular weight:225.291N-Phenethylbenzamide-d5
CAS:Controlled Product<p>Applications N-Phenethylbenzamide-d5 is an isotope labelled intermediate in the synthesis of deteurerium-labeled amides within microreactors.<br>References Hooper, J., Watts, P.: J. Labelled Compd. Rad., 50, 189 (2007)<br></p>Formula:C15H10D5NOColor and Shape:NeatMolecular weight:230.32







