90611-50-0

Upstream product

• 13756-98-4 (+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone 
• 13839-77-5 Ethyl 6-methyl-1,4-dioxaspiro[4.5]decane-6-carboxylate 
• 130735-18-1 2-Methoxymethoxymethyl-2,6-dimethylcyclohexanone 
• 130735-25-0 methyl 3-methoxymethoxymethyl-3-methyl-2-oxocyclohexanecarboxylate 
• 130735-26-1 methyl 3-methoxymethoxymethyl-1,3-dimethyl-2-oxocyclohexanecarboxylate 
• 130735-17-0 2-Methoxymethoxymethyl-2-methylcyclohexanone 
• 130735-16-9 2-Methoxymethoxymethyl-2-methylcyclohexanone Ethylene Acetal 
• 66088-37-7 ethyl 1-methyl-2-oxocyclohexancarboxylate 
• 87787-09-5 6-hydroxymethyl-6-methyl-1,4-dioxaspiro<4.5>decane 

Downstream Products

• 130735-21-6 1,3-Dimethyl-2-oxocyclohexanecarbaldehyde Ethylene Acetal 
• 164359-86-8 (+/-)-2-difluoromethyl-2,6-dimethyl-1-cyclohexanone 
• 130735-22-7 1,3-Dimethylcyclohex-2-ene-1,2-dicarbaldehyde 1-Ethylene Acetal 
• 130735-23-8 1,3-Dimethylcyclohex-2-ene-1,2-dicarbaldehyde 
• 164359-87-9 (+/-)-4-(1'-hydroxy-2'-difluoromethyl-2',6'-dimethylcyclohexyl)but-3-yn-2-ol-tetrahydropyranyl ether 
• 164359-89-1 (+/-)-3-(1'-hydroxy-2'-difluoromethyl-2',6'-dimethylcyclohexyl)-1-methyl-2-propynyl acetate 
• 164359-90-4 (+/-)-3-(2'-difluoromethyl-2',6'-dimethyl-1'-cyclohexen-1'-yl)-1-methyl-2-propynyl acetate 
• 164359-88-0 (+/-)-4-(1'-hydroxy-2'-difluoromethyl-2',6'-dimethylcyclohexyl)but-3-yn-2-ol 
• 164359-92-6 (+/-)-(E)-4-(6'-difluoromethyl-2',6'-dimethyl-1'-cyclohexen-1'-yl)-3-buten-2-one 

Relevant academic research and scientific papers

8',8'-DIFLUORO- AND 8',8',8'-TRIFLUOROABSCISIC ACIDS AS HIGHLY POTENT, LONG-LASTING ANALOGUES OF ABSCISIC ACID

Racemic 8',8'-difluoroabscisic acid (difluoro-ABA) and 8',8',8'-trifluoroabscisic acid (trifluoro-ABA) were synthesized as highly potent, long-lasting analogues of abscisic acid (ABA).The individual optical isomers were obtained by optical resolution of t

Total Synthesis of (+)-Perrottetianal A

The total synthesis of (+)-perrottetianal A, one of the sacculatane-type diterpenes isolated from liverworts, has been achieved starting from an optically active Wieland-Miescher ketone analogue.The ethylene glycol monoacetal of the starting material was