N-(2-Phenylethyl)benzolcarboxamid
N-(2-phenylethyl)benzamide
CAS: 3278-14-6
Molecular Formula: C15H15NO
N-(2-Phenylethyl)benzolcarboxamid - Names and Identifiers
| Name | N-(2-phenylethyl)benzamide |
| Synonyms | N-Phenethylbenzamide Solina New Impurity 21 N-(2-Phenethyl)benzamide N-(2-Phenylethyl)benzamid N-(2-phenylethyl)benzamide N-phenyl benzamide impurity Benzamide, N-(2-phenylethyl)- Benzeneethanamine, N-benzoyl- BenzaMide, N-(2-phenylethyl)- 4-(DICHLOROMETHYL)PYRIDINE HCL N-benzoyl-beta-phenylethylamine N-(2-Phenylethyl)benzolcarboxamid N-phenethylbenzamide (solina new impurity) Solifenacin Related Compound 21 (N-Phenethylbenzamide) |
| CAS | 3278-14-6 |
| EINECS | 248-592-1 |
| InChI | InChI=1/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) |
N-(2-Phenylethyl)benzolcarboxamid - Physico-chemical Properties
| Molecular Formula | C15H15NO |
| Molar Mass | 225.29 |
| Density | 1.088±0.06 g/cm3(Predicted) |
| Melting Point | 117-118 °C |
| Boling Point | 439.0±24.0 °C(Predicted) |
| Flash Point | 264.3°C |
| Vapor Presure | 6.61E-08mmHg at 25°C |
| pKa | 14.56±0.46(Predicted) |
| Refractive Index | 1.581 |
N-(2-Phenylethyl)benzolcarboxamid - Introduction
N-(2-phenylethyl)benzamide is an organic compound with the chemical formula C15H15NO. It is a white solid, odorless, insoluble in water and soluble in organic solvents such as ethanol and dichloromethane.
N-(2-phenylethyl)benzamide is commonly used in the fields of medicine and organic synthesis. In medicine, it is used as an antibacterial agent and drug intermediate, with antibacterial activity and anticancer activity. In organic synthesis, it can be used as a raw material for the synthesis of other compounds, such as substrates or catalysts for organic synthesis reactions.
The method for preparing N-(2-phenylethyl)benzamide can be obtained by the reaction of phenethylamine and benzoyl chloride. Briefly, phenethylamine is reacted with benzoyl chloride in a suitable solvent, usually at low temperature, and the product is purified by crystallization to give N-(2-phenylethyl)benzamide.
When using or handling N-(2-phenylethyl)benzamide, appropriate safety measures should be taken. It may be irritating to the skin and eyes, so protective gloves and goggles should be used. In addition, their inhalation and ingestion should be avoided. If necessary, operate in a well-ventilated environment and follow correct laboratory operating procedures.
N-(2-phenylethyl)benzamide is commonly used in the fields of medicine and organic synthesis. In medicine, it is used as an antibacterial agent and drug intermediate, with antibacterial activity and anticancer activity. In organic synthesis, it can be used as a raw material for the synthesis of other compounds, such as substrates or catalysts for organic synthesis reactions.
The method for preparing N-(2-phenylethyl)benzamide can be obtained by the reaction of phenethylamine and benzoyl chloride. Briefly, phenethylamine is reacted with benzoyl chloride in a suitable solvent, usually at low temperature, and the product is purified by crystallization to give N-(2-phenylethyl)benzamide.
When using or handling N-(2-phenylethyl)benzamide, appropriate safety measures should be taken. It may be irritating to the skin and eyes, so protective gloves and goggles should be used. In addition, their inhalation and ingestion should be avoided. If necessary, operate in a well-ventilated environment and follow correct laboratory operating procedures.
Last Update：2024-04-09 20:52:54
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View History
N-(2-Phenylethyl)benzolcarboxamid
10294-31-2
FMOC-GLU(BIOTINYL-PEG)-OH
4491-39-8
1805735-20-9
73940-88-2
938253-30-6
2H-Benzo[b]quinolizine-7-sulfonic acid, 1,3,4,6,11,11a-hexahydro-
4-(3-{2,4-bisnitrophenoxy}benzylidene)-2-(2-bromophenyl)-1,3-oxazol-5(4H)-one
10294-31-2
FMOC-GLU(BIOTINYL-PEG)-OH
4491-39-8
1805735-20-9
73940-88-2
938253-30-6
2H-Benzo[b]quinolizine-7-sulfonic acid, 1,3,4,6,11,11a-hexahydro-
4-(3-{2,4-bisnitrophenoxy}benzylidene)-2-(2-bromophenyl)-1,3-oxazol-5(4H)-one