141885-29-2

Upstream product

• 141885-16-7 3-methyl-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)phenyl acetate 
• 126727-42-2 3-methyl-5-(2',6',6'-trimethyl-1',3'-cyclohexadien-1'-yl)phenyl acetate 
• 126727-34-2 3-ethoxy-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-2-cyclohexen-1-one 
• 141885-13-4 3-methyl-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)phenol 
• 27259-15-0 5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)cyclohexane-1,3-dione 
• 127-41-3 alpha-ionone 
• 6550-94-3 3-methyl-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-2-cyclohexen-1-one 
• 126727-43-3 5-(1',2'-epoxy-2',6',6'-trimethyl-3'-cyclohexen-1'-yl)-3-methylphenyl acetate 

Downstream Products

• 141885-32-7 5-(1'-hydroxy-2',6',6'-trimethyl-4'-oxo-2'-cyclohexen-1'-yl)-3-methylphenol 

Relevant academic research and scientific papers

Synthesis of New Abscisic Acid (ABA) Analogs Possessing a Geometrically Rigid Cyclized Side Chain

In a solution, cis-abscisic acid (ABA) isomerizes into the trans-isomer which is physiologically inactive, and this structural instability is regarded as a reason for insuitability of ABA in agricultural applications.The side chain of ABA, the 2-cis-4-tra