141885-56-5

Upstream product

• 14203-64-6 7,9,9-trimethyl-1,4-dioxa-spiro[4.5]dec-6-en-8-one 
• 124-38-9 carbon dioxide 
• 1611-92-3 3,5-dibromotoluene 
• 141885-53-2 5-(1'-hydroxy-2',6',6'-trimethyl-4'-oxo-2'-cyclohexen-1'-yl)-3-methylbenzonitrile 
• 6550-94-3 3-methyl-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-2-cyclohexen-1-one 
• 127-41-3 alpha-ionone 
• 27259-15-0 5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)cyclohexane-1,3-dione 
• 141885-47-4 3-methyl-5-(2',6',6'-trimethyl-1',3'-cyclohexadien-1'-yl)benzonitrile 
• 141885-50-9 5-(1',2'-epoxy-2',6',6'-trimethyl-3'-cyclohexen-1'-yl)-3-methylbenzonitrile 
• 126727-34-2 3-ethoxy-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-2-cyclohexen-1-one 
• 141885-35-0 1-cyano-3-methyl-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-1,3-cyclohexadiene 
• 141885-38-3 3-methyl-5-(2',6',6'-trimethyl-2'-cyclohexen-1'-yl)benzonitrile 

Relevant academic research and scientific papers

One Pot Synthesis and Optical Resolution of Synthetic Mimic of Abscisic Acid Affecting Plant's Physiology

When conjugated dienic side chain of abscisic acid is substituted with 3-carboxyl-5-methylphenyl group, the product shows abscisic acid-like activity.We developed one pot synthetic pathway of it, which was optically resolved with chiral HPLC column.

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