35232-96-3

Basic information

• Product Name: 6-Methyl-5,7-dihydro-6H-dibenzo[c,e]azepine
• Synonyms: 6,7-Dihydro-6-methyl-5H-dibenz[c,e]azepine;6-Methyl-5,7-dihydro-6H-dibenzo[c,e]azepine;Ro-2-3176
• CAS NO: 35232-96-3
• Molecular Formula: C15H15N
• Molecular Weight: 0
• Mol File: 35232-96-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 337.9°C at 760 mmHg
• Flash Point: 143.4°C
• Appearance: /
• Density: 1.074g/cm³
• Vapor Pressure: 0.000102mmHg at 25°C
• Refractive Index: 1.6
• CAS DataBase Reference: 6-Methyl-5,7-dihydro-6H-dibenzo[c,e]azepine(CAS DataBase Reference)
• NIST Chemistry Reference: 6-Methyl-5,7-dihydro-6H-dibenzo[c,e]azepine(35232-96-3)
• EPA Substance Registry System: 6-Methyl-5,7-dihydro-6H-dibenzo[c,e]azepine(35232-96-3)

Safety Data

• Hazardous Substances Data: 35232-96-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H15N/c1-16-10-12-6-2-4-8-14(12)15-9-5-3-7-13(15)11-16/h2-9H,10-11H2,1H3

Upstream product

• 3433-80-5 1-Bromo-2-bromomethyl-benzene 
• 698-19-1 N-methyl-2-bromobenzylamine 
• 7375-70-4 N⁽¹⁾,N⁽²⁾-bis(2-bromobenzyl)-N⁽¹⁾,N⁽²⁾-dimethylpropane-1,3-diamine 
• 107-97-1 sarcosine 
• 1203-68-5 2-Phenylbenzaldehyde 
• 100891-94-9 N-methyl-5H-dibenzo[c,e]azepine-5,7(6H)-dione 
• 38274-14-5 2,2'-bis-(bromomethyl)-1,1'-biphenyl 
• 74-89-5 methylamine 
• 6050-13-1 biphenyl-2,2'-dicarboxylic acid anhydride 
• 3594-90-9 2,2'-bis(hydroxymethyl)biphenyl 

Relevant articles and documents

Hypolipidemic activity of 6-substituted 6,7-dihydro-5H-dibenz[c,e]azepine and the effects of 6,7-dihydro-5H-dibenz[c,e]azepine on lipid metabolism of rodents

A series of 6-substituted derivatives of 6,7-dihydro-5H-dibenz[c,e]azepine was found to be active hypolipidemic agents in rodents at doses of mg/kg per day. The parent drug was found to suppress the enzyme activity of ATP-dependent citrate lyase, sn-glyce

An amine template strategy to construct successive C-C bonds: Synthesis of benzo[: H] quinolines by a deaminative ring contraction cascade

We developed a convergent strategy to build, cyclize and excise nitrogen from tertiary amines for the synthesis of polyheterocyclic aromatics. Biaryl-linked azepine intermediates can undergo a deaminative ring contraction cascade reaction, excising nitrogen with the formation of an aromatic core. This strategy and deaminative ring contraction reaction are useful for the synthesis of benzo[h]quinolines. This journal is

1,7-Electrocyclisation of non-stabilised α,β:y,o-unsaturated azomethine ylides

The generation of α,β:γ,5-unsaturated azomethine ylides 8 is described, starting from TV-substituted α-amino acids 7 and aldehydes 6,12. These azomethine ylides undergo a 1,7-electrocyclisation, followed by a [l,5]-hydrogen shift, to give the dihydrobenza