57460-54-5

Basic information

• Product Name: 5,9,10-trimethyl-2,6-diazabicyclo[5.4.0]undeca-5,8,10,12-tetraen-3-one
• Synonyms: 5,9,10-trimethyl-2,6-diazabicyclo[5.4.0]undeca-5,8,10,12-tetraen-3-one;4,7,8-trimethyl-1,3-dihydro-1,5-benzodiazepin-2-one
• CAS NO: 57460-54-5
• Molecular Formula: C₁₂H₁₄N₂O
• Molecular Weight: 202.25236
• Mol File: 57460-54-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 398.1°Cat760mmHg
• Flash Point: 194.6°C
• Appearance: /
• Density: 1.17g/cm³
• Vapor Pressure: 1.51E-06mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: 5,9,10-trimethyl-2,6-diazabicyclo[5.4.0]undeca-5,8,10,12-tetraen-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5,9,10-trimethyl-2,6-diazabicyclo[5.4.0]undeca-5,8,10,12-tetraen-3-one(57460-54-5)
• EPA Substance Registry System: 5,9,10-trimethyl-2,6-diazabicyclo[5.4.0]undeca-5,8,10,12-tetraen-3-one(57460-54-5)

Safety Data

• Hazardous Substances Data: 57460-54-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14N2O/c1-7-4-10-11(5-8(7)2)14-12(15)6-9(3)13-10/h4-5H,6H2,1-3H3,(H,14,15)

Upstream product

• 674-82-8 4-methyleneoxetan-2-one 
• 3171-45-7 4,5-dimethyl-1,2-phenylenediamine 
• 141-97-9 ethyl acetoacetate 

Downstream Products

• 1200592-00-2 C₁₉H₂₇N₃O₂ 
• 1200592-09-1 C₂₀H₂₃N₃O₂ 
• 1200592-06-8 C₂₁H₂₅N₃O₂ 

Relevant articles and documents

Novel syntheses of tetrahydrobenzodiazepines and dihydropyrazines via isocyanide-based multicomponent reactions of diamines

In this work, two novel isocyanide-based mul multicomponent reactions of 1,2-diamine compounds with diketene have been developed as efficient strategies for the synthesis of 2,3,4,5-tetrahydro-lH-benzo[b][l,4]diazepine2-carboxamidcs with regiochemical control and 1,6-dihydropyrazinc-2,3-dicarbonitrilcs in good to excellent yields at ambient temperature.

Synthese et reactivite de nouvelles molecules de type bis--1,n alcanes

A number of bis-1,n- alkanes have been prepared by reaction between 4-phenyl (4-cyclopropyl and 4-methyl)-2,3-dihydro 1,5-benzodiazepine 2-one and dihalogenoalkanes X-(CH2)n-X under phase transfer catalysis conditions.The action of hydrazine at different concentration on this structure have been studied.These products have been characterized by NMR 1H, IR, MS and the microanalysis.