Phthalimide, N-benzyl-
Phthalimide, N-benzyl- structure
|
Common Name | Phthalimide, N-benzyl- | ||
|---|---|---|---|---|
| CAS Number | 2142-01-0 | Molecular Weight | 237.253 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 393.0±21.0 °C at 760 mmHg | |
| Molecular Formula | C15H11NO2 | Melting Point | 114-116 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 179.8±14.4 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
Novel and versatile methodology for synthesis of cyclic imides and evaluation of their cytotoxic, DNA binding, apoptotic inducing activities and molecular modeling study.
Eur. J. Med. Chem. 42 , 614-26, (2007) Versatile method has been developed for synthesis of N-substituted imides. Thus, acid anhydrides, imides and dicarboxylic acids were successfully subjected to dehydrative cyclization with substituted amines using DPPOx and Et(3)N to afford N-substituted imide... |
|
|
Inhibition of monoamine oxidase by C5-substituted phthalimide analogues.
Bioorg. Med. Chem. 19 , 4829-40, (2011) Literature reports that isatin as well as C5- and C6-substituted isatin analogues are reversible inhibitors of human monoamine oxidase (MAO) A and B. In general, C5- and C6-substitution of isatin leads to enhanced binding affinity to both MAO isozymes compare... |
|
|
N-benzylphthalimide. Warzecha K-D, et al.
Acta Crystallogr. Sect. E Struct. Rep. Online 62(6) , 2367-68, (2006)
|
|
|
Impact of molecular size on electron spin relaxation rates of nitroxyl radicals in glassy solvents between 100 and 300 K. Sato HIDEO, et al.
Mol. Phys. 105(15-16) , 2137-51, (2007)
|
|
|
Highly fluorous porphyrins as model compounds for molecule interferometry. Tüxen J, et al.
European J. Org. Chem. 25 , 4823-33, (2011)
|
|
|
Vibrational assignment of N-benzylphthalimide and 15N-benzylphthalimide. Kolev T and Juchnovski I.
J. Mol. Struct. 349 , 377-380, (1995)
|
|
|
The direct conversion of phthalimides to isoindoles. Garmaise DL and Ryan A.
J. Heterocycl. Chem. 7(2) , 413, (1970)
|