| Identification | Back Directory | [Name]
1-METHYL-5-PHENYL-1,3-DIHYDRO-BENZO[E][1,4]DIAZEPIN-2-ONE | [CAS]
3034-65-9 | [Synonyms]
Ro-5-3464
1-Methyl-5-phenyl-1H-1,4-benzodiazepine-2(3H)-one
1-Methyl-5-[phenyl]-1H-1,4-benzodiazepin-2(3H)-one
1-methyl-2,3-dihydro-2-oxo-5-phenyl-1,4-benzodiazepine
1,3-Dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one
1-METHYL-5-PHENYL-1,3-DIHYDRO-BENZO[E][1,4]DIAZEPIN-2-ONE
1-Methyl-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepine-2-one
2H-1,4-Benzodiazepin-2-one, 1,3-dihydro-1-methyl-5-phenyl-
1-Methyl-5-phenyl-1,3-dihydro-2H-benzo[e][1,4]diazepin-2-one | [Molecular Formula]
C16H14N2O | [MDL Number]
MFCD01314158 | [MOL File]
3034-65-9.mol | [Molecular Weight]
250.3 |
| Chemical Properties | Back Directory | [Melting point ]
153 °C | [Boiling point ]
452.3±45.0 °C(Predicted) | [density ]
1.15±0.1 g/cm3(Predicted) | [solubility ]
DMSO: Slightly soluble: 0.1-1 mg/ml
Ethanol: Slightly soluble: 0.1-1 mg/ml | [form ]
Solid | [pka]
3.62±0.50(Predicted) | [color ]
Light yellow to brown |
| Hazard Information | Back Directory | [Uses]
Deschlorodiazepam is an analytical reference standard categorized as a benzodiazepine[1][2]. | [References]
[1] Basile AS, et al. Brain concentrations of benzodiazepines are elevated in an animal model of hepatic encephalopathy. Proc Natl Acad Sci U S A. 1990 Jul;87(14):5263-7. DOI:10.1073/pnas.87.14.5263
[2] Sternbach LH, et al. Quinazolines and 1,4-benzodiazepines. 64. Comparison of the stereochemistry of diazepam with that of close analogs with marginal biological activity. J Med Chem. 1974 Mar;17(3):374-7. DOI:10.1021/jm00249a032 |
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