28707-60-0

Basic information

• Product Name: Quinoline, 5,6,7,8-tetrahydro-8-(phenylmethylene)-
• CAS NO: 28707-60-0
• Molecular Formula: C16H15N
• Molecular Weight: 221.302
• Mol File: 28707-60-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Quinoline, 5,6,7,8-tetrahydro-8-(phenylmethylene)-(CAS DataBase Reference)
• NIST Chemistry Reference: Quinoline, 5,6,7,8-tetrahydro-8-(phenylmethylene)-(28707-60-0)
• EPA Substance Registry System: Quinoline, 5,6,7,8-tetrahydro-8-(phenylmethylene)-(28707-60-0)

Safety Data

• Hazardous Substances Data: 28707-60-0(Hazardous Substances Data)

Upstream product

• 10500-57-9 5,6,7,8-tetrahydroquinoline 
• 108-24-7 acetic anhydride 
• 100-52-7 benzaldehyde 
• 111113-91-8 8-Benzyliden-5,6,7,8-tetrahydrochinolinium-1-(ethoxycarbonylaminid) 

Downstream Products

• 28748-06-3 8-benzyl-5,6,7,8-tetrahydro-quinoline 
• 56826-69-8 5,6,7,8-tetrahydro-8-quinolinone 
• 67046-22-4 5,6,7,9-tetrahydro-8H-pyrido[2,3-b]azepin-8-one 
• 864829-37-8 7-[4-(2-methylphenyl)piperidine-1-carbonyl]-5,6,7,8-tetrahydrocyclohepta[b]pyridine-9-one 
• 58509-59-4 6,7-dihydro-5H-quinolin-8-one oxime 
• 864829-41-4 (-)-((7R,9S)-9-{[tert-butyl(dimethyl)silyl]oxy}-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-7-yl)methyl 4-methylbenzenesulfonate 
• 111113-91-8 8-Benzyliden-5,6,7,8-tetrahydrochinolinium-1-(ethoxycarbonylaminid) 
• 111113-96-3 1-Amino-8-benzyliden-5,6,7,8-tetrahydrochinolinium-mesitylensulfonat 

Relevant articles and documents

Polyaza Cavity Shaped Molecules. Annelated Derivatives of 2-(2'-Pyridyl)-1,8-naphthyridine and 2,2'-Bi-1,8-naphthyridine

A two-step method is presented for the oxidation of the 2-methylene position of 2,3-cycloalkenopyridines.The pyridyl ketones thus obtained may be reacted with 2-aminonicotinaldehyde to yield 3,3'-annelated derivatives of 2-(2'-pyridyl)-1,8-naphthyridine.T

QUINOLYNYLMETHYLIMIDIZOLES AS THERAPEUTIC AGENTS

Disclosed herein is a compound of the formula (I):(I).Therapeutic methods, compositions and medicaments related thereto are also disclosed.

A facile synthesis of α,α′-bis(substituted-benzylidene)-cycloalkanones and substituted-benzylidene heteroaromatics: utility of NaOAc as a catalyst for aldol-type reaction

Utility of NaOAc in glacial HOAc as a catalyst for aldol-type condensation reactions was examined. Reactions of cycloalkanones and selected heteroaromatics with various aldehydes in the presence of NaOAc in glacial HOAc provided α,α′-bis(substituted-benzylidene)cycloalkanones and substituted-benzylidene heteroaromatics, respectively, in good yields.