369610-41-3

Basic information

• Product Name: 1,1,2-trimethyl-2-(2-methoxymethyloxy-5-methylphenyl)cyclopentane
• Synonyms: 1,1,2-trimethyl-2-(2-methoxymethyloxy-5-methylphenyl)cyclopentane
• CAS NO: 369610-41-3
• Molecular Weight: 262.392
• Mol File: 369610-41-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,1,2-trimethyl-2-(2-methoxymethyloxy-5-methylphenyl)cyclopentane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2-trimethyl-2-(2-methoxymethyloxy-5-methylphenyl)cyclopentane(369610-41-3)
• EPA Substance Registry System: 1,1,2-trimethyl-2-(2-methoxymethyloxy-5-methylphenyl)cyclopentane(369610-41-3)

Safety Data

• Hazardous Substances Data: 369610-41-3(Hazardous Substances Data)

Upstream product

• 369610-36-6 (1R,2S)-1-(hydroxymethyl)-2-(2-methoxy-5-methylphenyl)-1,2-dimethylcyclopentane 
• 369610-30-0 2-iodo-4-methylphenyl 1,2-dimethyl-2-cyclopentenecarboxylate 
• 369610-32-2 epi-herbertenolide 
• 369610-38-8 1,2-dimethyl-1-formyl-2-(2-methoxy-5-methylphenyl)cyclopentane 
• 325726-91-8 1,2-dimethyl-1-hydroxymethyl-2-(2-hydroxy-5-methylphenyl)cyclopentane 
• 175520-10-2 (R)-1,2-dimethyl-2-cyclopentenecarboxylate 
• 162489-18-1 methyl (R)-1-methyl-2-oxocyclopentanecarboxylate 
• 81784-13-6 (1S)-1,2,2-trimethyl-1-(2-methoxy-5-methyl)phenylcyclopentane 
• 138200-47-2 N-(2-carbomethoxy-1-cyclopenten-1-yl)-(S)-valine tert-butyl ester 
• 81784-10-3 4-methyl-2-[(1S)-1,2,2-trimethylcyclopentyl]phenol 
• 107-30-2 chloromethyl methyl ether 

Downstream Products

• 86996-95-4 (S)-5-methyl-3-(1,2,2-trimethylcyclopentyl)benzene-1,2-diol 
• 124424-22-2 (-)-mastigophorene B 
• 369610-42-4 1,1,2-trimethyl-2-(3-hydroxy-2-methoxymethyloxy-5-methylphenyl)cyclopentane 

Relevant articles and documents

Total syntheses of neuroprotective mastigophorenes A and B

(-)-Herbertenediol (3) which is regarded as a biosynthetic precursor of mastigophorenes A and B has been effectively synthesized from (R)-1,2-dimethyl-2-cyclopentene carboxylic acid by applying an intramolecular Heck reaction to the construction of the quaternary carbon center, and then horseradish peroxidase-catalyzed oxidative coupling of 3 has given rise to (-)-mastigophorenes A and B. Mastigophorenes A and B have been found to exhibit significant neuroprotective activity in primary cultures of fetal rat cortical neurons.