1061330-08-2

Basic information

• Product Name: (R)-4-(4-methoxyphenylmethoxy)cyclopent-2-enone
• Synonyms: (R)-4-(4-methoxyphenylmethoxy)cyclopent-2-enone
• CAS NO: 1061330-08-2
• Molecular Weight: 218.252
• Mol File: 1061330-08-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-4-(4-methoxyphenylmethoxy)cyclopent-2-enone(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-(4-methoxyphenylmethoxy)cyclopent-2-enone(1061330-08-2)
• EPA Substance Registry System: (R)-4-(4-methoxyphenylmethoxy)cyclopent-2-enone(1061330-08-2)

Safety Data

• Hazardous Substances Data: 1061330-08-2(Hazardous Substances Data)

Upstream product

• 1514903-06-0 (1R,4R)-4-((4-methoxybenzyl)oxy)cyclopent-2-enol 
• 40630-12-4 1,5-dichloropentane-2,4-dione 
• 136030-28-9 (2R,4R)-1,5-dichloropentane-2,4-diol 
• 824-94-2 p-methoxybenzyl chloride 
• 1477979-57-9 (1S,4R)-1-acetyloxy-4-(4-methoxyphenylmethoxy)cyclopent-2-ene 
• 1477979-50-2 (RS)-4-(4-methoxyphenylmethoxy)cyclopent-2-enone 
• 59995-47-0 4-Hydroxycyclopent-2-enone 
• 98-00-0 (2-furyl)methyl alcohol 
• 1061330-05-9 (1S,4R)-4-(4-methoxyphenylmethoxy)cyclopent-2-enol 

Downstream Products

• 1061330-09-3 (R)-2-bromo-4-(4-methoxyphenylmethoxy)cyclopent-2-enone 
• 1061330-14-0 2-[(1S,5R)-2-bromo-3-[(1,1-dimethylethyl)dimethylsilyloxy]-5-(4-methoxyphenylmethoxy)cyclopent-2-enyl]acetaldehyde 
• 1061330-15-1 (3R,4S)-2-bromo-1-[(1,1-dimethylethyl)dimethylsilyloxy]-4-(4-(methoxyphenyl)methoxy)-3-((Z)-oct-2-enyl)cyclopent-1-ene 
• 1061330-18-4 4-[(2R,3R)-3-((E)-((2R,3R)-3-(4-methoxyphenylmethoxy)-2-((Z)-oct-2-enyl)-5-oxo-cyclopentylidene)methyl)oxiran-2-yl]butanal 
• 1061330-20-8 4-[(2R,3R)-3-((E)-((2R,3R)-3-(4-methoxyphenylmethoxy)-2-((Z)-oct-2-enyl)-5-oxo-cyclopentylidene)methyl)oxiran-2-yl]butanoic acid 

Relevant articles and documents

Stereodivergent synthesis of enantioenriched 4-hydroxy-2-cyclopentenones

Protected 4-hydroxycyclopentenones (4-HCPs) constitute an important class of intermediates in chemical synthesis. A route to this class of compound has been developed. Key steps include Noyori reduction (which establishes the stereochemistry of the produc

Improved synthesis of the epoxy isoprostane phospholipid PEIPC and its reactivity with amines

(Chemical Equation Presented) An improved synthesis of the naturally occurring hydroxy ketone 1-palmitoyl-2-(5,6)-epoxyisoprostane E 2-sn-glycero-3-phosphocholine (PEIPC) 1, a compound that plays a role in endothelial activation in atherosclerosis, has been carried out using a PMB ether as the key protecting group. Opening of an intermediate with pentylamine shows that the allylic epoxide is the position of attack by nucleophiles.