939-78-6

Basic information

• Product Name: Benzene, [(2,2-dichlorocyclopropyl)methyl]-
• CAS NO: 939-78-6
• Molecular Formula: C10H10Cl2
• Molecular Weight: 201.095
• Mol File: 939-78-6.mol

Chemical Properties

• CAS DataBase Reference: Benzene, [(2,2-dichlorocyclopropyl)methyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [(2,2-dichlorocyclopropyl)methyl]-(939-78-6)
• EPA Substance Registry System: Benzene, [(2,2-dichlorocyclopropyl)methyl]-(939-78-6)

Safety Data

• Hazardous Substances Data: 939-78-6(Hazardous Substances Data)

Upstream product

• 300-57-2 allylbenzene 
• 67-66-3 chloroform 

Downstream Products

• 56058-23-2 2,2-dimethoxy-5-phenyl-2,3-dihydrofuran 
• 56058-24-3 2,2-diphenoxy-5-phenyl-2,3-dihydro-furan 
• 120383-86-0 trifluoroacetate of 1-phenyl-2-butanol 
• 56058-25-4 1-benzoyl-2,2-di(phenylthio)cyclopropane 
• 120383-85-9 1-(cyclopropylmethyl)-4-nitrobenzene 
• 120383-87-1 formate of 1-phenyl-2-butanol 
• 120383-88-2 trifluoroacetate of 1-(o-nitrophenyl)-2-butanol 
• 120383-89-3 trifluoroacetate of 1-(p-nitrophenyl)-2-butanol 
• 56058-27-6 trans-1-Benzoyl-2-chlorocyclopropane 
• 56058-27-6 cis-1-Benzoyl-2-chlorocyclopropane 
• 120383-84-8 (2-nitrobenzyl)cyclopropane 
• 1327334-73-5 4-benzyl-5-chloroisoxazole 
• 882817-20-1 2-(2-nitrobenzyl)-1-chlorocyclopropane 
• 56058-26-5 2-benzyl-1-chlorocyclopropane 

Relevant articles and documents

BENZYL- and 2- AND 4-NITROBENZYLCYCLOPROPANES AND THEIR REACTION WITH ORGANIC ACIDS

The nitration of benzylcyclopropane and its transformations in organic acids were studied.Under the conditions of electrophilic nitration the small ring is preserved, while the ratio of the o- and p-nitrophenyl derivatives amounts to 1.1:1.The reaction of benzylcyclopropane with formic and acetic acids takes place with the addition of the fragments of the acids at the 1,2-bond of the three-carbon ring; o- and p-nitrobenzylcyclopropanes do not react with formic and acetic acids, with trifluoroacetic acid they form trifluoroacetates, and in the case of the ortho-substituted isomer nucleophilic assistance from the nitro group is observed.