| Bioactivity | N-Phenylbenzamide (N-Benzoylaniline) exhibits high rectification and high conductance. N-Phenylbenzamide is utilized to manufacture dyes, pigments, perfumes and other aromatic compounds[1][2]. | ||||||||||||
| CAS | 93-98-1 | ||||||||||||
| Formula | C13H11NO | ||||||||||||
| Molar Mass | 197.23 | ||||||||||||
| Appearance | 固体 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
|
||||||||||||
| Reference | [1]. Ding W, et al., Computational Design of Intrinsic Molecular Rectifiers Based on Asymmetric Functionalization of N-Phenylbenzamide. J Chem Theory Comput. 2015 Dec 8;11(12):5888-96. [2]. Matos M A R, Miranda M S, Morais V M F, et al. Benzanilide: on the crossroads of calorimetry, computations and concepts[J]. Molecular Physics, 2006, 104(18): 2855-2860. |
N-Phenylbenzamide
CAS: 93-98-1 F: C13H11NO W: 197.23
N-Phenylbenzamide (N-Benzoylaniline) exhibits high rectification and high conductance. N-Phenylbenzamide is utilized to
Sales Email：peptidedb@qq.com
This product is for research use only, not for human use. We do not sell to patients.