155638-29-2

Upstream product

• 57188-99-5 3-butyn-2-yl tetrahydropyranyl ether 
• 2816-57-1 2,6-dimethylcyclohexanone 
• 13756-97-3 (+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone ethylene ketal 
• 13756-98-4 (+/-)-2-hydroxymethyl-2,6-dimethyl-1-cyclohexanone 

Downstream Products

• 155638-32-7 (+/-)-3-(2'-methoxymethyl-2',6'-dimethyl-1'-cyclohexene-1'-yl)-1-methyl-2-propynyl acetate 
• 155638-31-6 (+/-)-3-(1'-hydroxy-6'-methoxymethyl-2',6'-dimethylcyclohexyl)-1-methyl-2-propynyl acetate 
• 155638-34-9 (+/-)-4-(6'-methoxymethyl-2',6'-dimethyl-1'-cyclohexene-1'-yl)-3-buten-2-one 
• 155638-30-5 (+/-)-4-(1'-hydroxy-2'-methoxymethyl-2',6'-dimethylcyclohexyl)-but-3-yn-2-ol 

Relevant academic research and scientific papers

8'- and 9'-Methoxyabscisic Acids as Antimetabolic Analogs of Abscisic Acid

8'- and 9'-Methoxyabscisic acids (methoxy-ABAs) were synthesized as antimetabolic analogs of abscisic acid (ABA).The racemic mixtures were resolved by HPLC. (+)-8'-Methoxy-ABA inhibited the elongation of rice seedling four times more strongly than (+)-ABA did, and (+)-9'-methoxy-ABA inhibited the germination of lettuce seeds and the induction of α-amylase by gibberellin A3 in barley seeds seven and two times more strongly, respectively.These methoxy-ABAs are the first analogs reported to have higher activity than ABA. (+)-8'- and (+)-9'-Methoxy-ABAs were less active in causing stomatal closure than (+)-ABA.These biological activities and 1H-NMR analysis suggest that the activity of methoxy-ABAs involved delayed metabolism, as was expected.The activity of (-)-isomers of ABA and methoxy-ABAs was also tested.