67913-78-4

Basic information

• Product Name: Benzo[h]quinoline, 5,6-dihydro-2,4-diphenyl-
• CAS NO: 67913-78-4
• Molecular Formula: C25H19N
• Molecular Weight: 333.433
• Mol File: 67913-78-4.mol
• Article Data: 21

Chemical Properties

• CAS DataBase Reference: Benzo[h]quinoline, 5,6-dihydro-2,4-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzo[h]quinoline, 5,6-dihydro-2,4-diphenyl-(67913-78-4)
• EPA Substance Registry System: Benzo[h]quinoline, 5,6-dihydro-2,4-diphenyl-(67913-78-4)

Safety Data

• Hazardous Substances Data: 67913-78-4(Hazardous Substances Data)

Upstream product

• 110-91-8 morpholine 
• 76017-39-5 1-benzyl-5,6-dihydro-2,4-diphenylbenzoquinolinium trifluoromethanesulphonate 
• 109-06-8 α-picoline 
• 75864-90-3 N-benzyl-5,6-dihydro-2,4-diphenylbenzo quinolinium tetrafluoroborate 
• 71-41-0 pentan-1-ol 
• 920-66-1 1,1,1,3',3',3'-hexafluoro-propanol 
• 71451-97-3 C₃₁H₂₄N⁽¹⁺⁾*CNS^(1-) 
• 28353-74-4 3,4-dihydronaphthalen-1(2H)-one O-acetyl oxime 
• 358621-92-8 N-(p-tolylsulfonyl)-1,3-diphenyl-2-propen-1-imine 
• 110-86-1 pyridine 
• 529-34-0 3,4-dihydronaphthalene-1(2H)-one 
• 7338-94-5 1,3-diphenyl-2-propynone 
• 94-41-7 benzalacetophenone 

Relevant articles and documents

Kinetics and Mechanism of Nucleophilic Displacements with Heterocycles as Leaving Groups. Part 11. ρ* Plots for the Solvolysis of 1-s-Alkyl-5,6-dihydro-2,4-diphenylbenzoquinolinium Cations.

The ρ* values for (1c-h) for (i) solvolysis in trifluoroacetic acid (-5.7), (ii) for solvolysis in pentanol (-1.2), and (iii) for unimolecular reaction with piperidine in chlorobenzene (-3.1) are discussed with respect to (a) the hypothesis tha

Method for synthesizing polysubstituted pyridine derivative based on oxime ester and unsaturated ketone under catalysis of ferric salt

The invention belongs to the technical field of organic synthesis, and particularly relates to a method for synthesizing a polysubstituted pyridine derivative based on oxime ester and unsaturated ketone under the catalysis of ferric salt. For the first ti

Synthesis of Highly Substituted Pyridines through Copper-Catalyzed Condensation of Oximes and α,β-Unsaturated Imines

A copper-catalyzed condensation reaction of oxime acetates and α,β-unsaturated ketimines to give pyridine derivatives is reported. The reaction features mild conditions, high functional-group compatibility, and high regioselectivity with respect to unsymmetrical oxime acetates, thus allowing the preparation of a wide range of polysubstituted pyridines, many of which are not readily accessible by conventional condensation methods.