156006-03-0

Basic information

• Product Name: 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester
• Synonyms: 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester
• CAS NO: 156006-03-0
• Molecular Weight: 311.404
• Mol File: 156006-03-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester(156006-03-0)
• EPA Substance Registry System: 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 2-thioxo-2H-pyridin-1-yl ester(156006-03-0)

Safety Data

• Hazardous Substances Data: 156006-03-0(Hazardous Substances Data)

Upstream product

• 156006-06-3 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid 
• 1121-31-9 2-mercaptopyridine N-oxide 
• 55285-80-8 ethyl 2-oxo-1-phenylcyclopentane-1-carboxylate 
• 156006-04-1 1-Phenyl-cyclopent-2-enecarboxylic acid ethyl ester 
• 156006-05-2 2-Phenyl-bicyclo[3.1.0]hexane-2-carboxylic acid ethyl ester 

Downstream Products

• 771-98-2 1-Phenylcyclohexene 
• 57497-04-8 3-Methyl-1-phenylcyclopent-1-ene 

Relevant articles and documents

Kinetic Analysis of the Rearrangement of a Conformationally Constrained α-Cyclopropylbenzyl Radical

Modulation of the cyclopropylmethyl (CPM)/homoallyl radical equilibrium by phenyl substitution at the radical center is exploited in determining the kinetic versus thermodynamic preference for bond scission in a bicyclic CPM radical.Exocyclic ring opening is determined to be 28.7 times faster than the respective endocyclic process.This method will be of general use for determining the regioselectivity of radical rearrangements.