125136-36-9

Upstream product

• 20445-31-2 R-(+)-α-trifluoromethyl-α-methoxy-phenylacetic acid 
• 125224-45-5 trans-(1S,2R)-(+)-2-(4-methoxybenzyl)-1-cyclohexanol 
• 39637-99-5 (S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride 
• 84654-70-6 trans-2-(4-methoxybenzyl)cyclohexyl acetate 
• 37722-51-3 (+/-)-trans-2-(4-methoxybenzyl)cyclohexan-1-ol 
• 950835-56-0 (1S,2R)-2-(4-methoxybenzyl)cyclohexyl butanoate 

Relevant academic research and scientific papers

Insect pest control agents: Novel chiral butanoate esters (juvenogens)

During the investigation of ester derivatives (juvenogens, biochemically activated insect hormonogenic compounds) of biologically active alcohols with potential application in insect pest control, a need for availability of all existing stereoisomers of e

Application of ionic liquids in enzymic resolution by hydrolysis of cycloalkyl acetates

A comparative study was performed in the enzymic resolution of the isomers of 2-(4-methoxybenzyl)cyclohexyl acetates 1 and 2. The investigation consisted in application of three commercially available lipases (Novozyme 435, Lipozyme IM and non-immobilized

BIOTRANFORMATION OF 2-(4-METHOXYBENZYL)-1-CYCLOHEXANONE BY MEANS OF Saccharomyces cerevisiae

Biotranformation reduction of 2-(4-methoxybenzyl)-1-cyclohexanone was investigated.A method was elaborated for the preparation of some diastereoisomeric alcohols derived from the racemic title ketone and for the determination of the products obtained.The

DIRECT ESTERIFICATION OF α-METHOXY-α-(TRIFLUOROMETHYL)PHENYLACETIC ACID

Esters of α-methoxy-α-(trifluoromethyl)phenylacetic acid (Mosher acid, MTPA) were prepared in good yields from alcohols and the free acid Ia using 2-chloro-1-methylpyridinium iodide (II) as condensing agent.