929721-54-0

Basic information

• Product Name: (meso)-2,5-diphenylcyclopentane-1,1-dicarboxylic acid diethyl ester
• Synonyms: (meso)-2,5-diphenylcyclopentane-1,1-dicarboxylic acid diethyl ester
• CAS NO: 929721-54-0
• Molecular Weight: 366.457
• Mol File: 929721-54-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (meso)-2,5-diphenylcyclopentane-1,1-dicarboxylic acid diethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (meso)-2,5-diphenylcyclopentane-1,1-dicarboxylic acid diethyl ester(929721-54-0)
• EPA Substance Registry System: (meso)-2,5-diphenylcyclopentane-1,1-dicarboxylic acid diethyl ester(929721-54-0)

Safety Data

• Hazardous Substances Data: 929721-54-0(Hazardous Substances Data)

Upstream product

• 41570-67-6 1-benzyltetrahydro-1H-thiophen-1-ium bromide 
• 100-39-0 benzyl bromide 
• 495-71-6 phenacylacetophenone 
• 2085-90-7 1,4-diphenyl-1,4-butanediol 
• 82631-96-7 1,4-diphenyl-1,4-butanediol bis(methanesulfonic acid ester) 
• 105-53-3 diethyl malonate 
• 100-51-6 benzyl alcohol 

Downstream Products

• 929721-56-2 (meso)-2,5-diphenylcyclopentane-1,1-dimethanol 

Relevant articles and documents

Asymmetric sulfur-ylide-mediated formal [4+1]-annulation reaction: Scope and mechanism

A formal [4+1]-annulation strategy between sulfur ylides and 1,3-dienes was developed to afford functionalized cyclopentanoids. The process consists of a stereoselective cyclopropanation reaction followed, in situ, by a stereospecific MgI2-cata

Synthesis and characterization of new chiral palladium β-diimine complexes

The synthesis and characterization of a range of chiral β-diimine ligands and their complexes with palladium(II) has been investigated. The introduction of chirality can be easily achieved through a combination of both achiral and chiral building blocks.