35134-49-7

Upstream product

• 35022-93-6 2-benzylidene-6-(1-cyclohexenyl)-1-cyclohexanone 
• 5682-83-7 2-Benzylidenecyclohexanone 
• 5682-83-7 (E)-2-benzylidenecyclohexanone 
• 897-78-9 2,6-bis(benzylidene)cyclohexanone 
• 108-94-1 cyclohexanone 
• 100-52-7 benzaldehyde 
• 1502-22-3 2-(1-cyclohexenyl)cyclohexanone 

Relevant academic research and scientific papers

Special reactions of α,β-unsaturated ketones III [1]. Formation and structure elucidation of dimers of 2-aryl-methyleneketones: (5E)-5-benzylidene-9β-phenyl-trans-4a-1,2,3,4,4a,5,6,7,8,9a- decahydroxanthen-4aα-ol and 3β,5β-bis-(4-methoxyphenyl)-2α,4β,6α-t

The reaction of 2-benzylidenecyclohexanone and 1-(4-methoxyphenyl)-2-methyl-1-penten-3-one with guanidine did not yield the expected 4-phenylhexahydro-2-quinazolinamine and 4-(p-methoxyphenyl)-dihydro-2-pyrimidinamine, respectively, but nitrogen-free prod

CONDENSATION OF ALDEHYDES AND KETONES. XIII. ALKALINE CONDENSATION OF 2-(1-CYCLOHEXENYL)-1-CYCLOHEXANONE WITH BENZALDEHYDE

The alkaline condensation of 2-(1-cyclohexenyl)-1-cyclohexanone with benzaldehyde was investigated with the initial compounds in various molar ratios.The isomeric products from the reaction of the ketone molecule with one and two molecules of the aldehyde and also 5-benzylidene-4a-hydroxy-9-phenyl-4-(1-cyclohexenyl)-1,2,3,4,4a,5,6,7,8,9a-decahydroxanthene were obtained.