134435-46-4

Upstream product

• 22532-51-0 4-methoxyphenethyl acetate 
• 75-36-5 acetyl chloride 
• 702-23-8 2-(4-Methoxyphenyl)ethanol 

Downstream Products

• 134435-52-2 7-cyano-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-55-5 2-Benzenesulfinyl-7-isopropyl-6-methoxy-1,1,4a-trimethyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 
• 61494-73-3 12-hydroxy-abieta-8,11,13-trien-3,7-dione 
• 2944-47-0 o-isopropylanisole 
• 187161-51-9 3-Isopropoxy-6-[2-(3-isopropyl-4-methoxy-phenyl)-ethyl]-5,5-dimethyl-cyclohex-2-enone 
• 134435-49-7 1-isopropyl-4-methoxyphenylethyl acetate 
• 187161-50-8 1-isopropyl-4-methoxyphenylethyl iodide 
• 134435-48-6 3-(1-methylethenyl)-4-methoxyphenylethyl acetate 
• 39863-70-2 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol 
• 134435-47-5 3-(1-hydroxy-1-methylethyl)-4-methoxyphenylethanol 

Relevant academic research and scientific papers

Highly Chemoselective gem-Difluoropropargylation of Aliphatic Alcohols

Despite the potential of α-fluoroethers in medicinal chemistry, their synthetic methods, especially etherification of aliphatic alcohols, have been limited. Herein, we developed two- and three-step gem-difluoropropargylation of aliphatic alcohols includin

N-ALKOXYALKYL-N,N-DIALKYLAMINE DERIVATIVES OR SALTS THEREOF, AND REMEDIES FOR NERVE DEGENERATION DISEASES CONTAINING THE SAME

An N-alkoxyalkyl-N,N-dialkylamine derivative represented by the following general formula [1]: wherein the ring D represents a 5- or 6-membered heterocyclic ring or hydrocarbon ring; R3 and R4, which are the same or different, represent an unsubstituted or substituted alkyl, cycloalkyl or aralkyl group; and R1, R2, R5, R6, R7, R8, m and n are as defined in the specification, or a salt thereof has an anti-hypoxic activity, a nerve-protecting activity and a nerve regeneration promoting activity and is useful for the treatment of neurodegenerative diseases.

Synthesis of 12-O-methyl-2a-methoxyferruginol

A rapid synthesis of 12-O-methyl-2-methoxyferruginol (1) shows it not to be identical with the natural product ascribed this structure.

Synthesis of aromatic diterpenes synthesis of 12-hydroxy-abieta-8,11,13-trien-3,7-dione

Model studies involving cationic cyclisation of suitable dienes have provided a synthesis of the title compound. Preparation of the dienes from available aromatic starting materials and the modification of the cyclised products are described.