78072-76-1

Basic information

• Product Name: 1-[4-(2-CHLOROCYCLOPROPYL)PHENYL]ETHAN-1-ONE
• Synonyms: 1-[4-(2-CHLOROCYCLOPROPYL)PHENYL]ETHAN-1-ONE
• CAS NO: 78072-76-1
• Molecular Formula: C₁₁H₁₁ClO
• Molecular Weight: 194.66
• Mol File: 78072-76-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 45 °C
• Appearance: /
• CAS DataBase Reference: 1-[4-(2-CHLOROCYCLOPROPYL)PHENYL]ETHAN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[4-(2-CHLOROCYCLOPROPYL)PHENYL]ETHAN-1-ONE(78072-76-1)
• EPA Substance Registry System: 1-[4-(2-CHLOROCYCLOPROPYL)PHENYL]ETHAN-1-ONE(78072-76-1)

Safety Data

• Hazardous Substances Data: 78072-76-1(Hazardous Substances Data)

Upstream product

• 29667-51-4 1-chloro-2-phenylcyclopropane 
• 75-36-5 acetyl chloride 
• 17651-00-2 (2-chlorocyclopropyl)benzene 
• 17650-99-6 (2-chlorocyclopropyl)benzene 

Downstream Products

• 137601-76-4 p-(cis-2-Chlorocyclopropyl)-α-methylbenzyl Chloride 
• 80857-72-3 cis-1-chloro-2-(4-cinnamoylphenyl)cyclopropane 
• 78072-81-8 1-((1S,2S)-2-Chloro-cyclopropyl)-4-isopropenyl-benzene 
• 137601-76-4 p-(trans-2-Chlorocyclopropyl)-α-methylbenzyl Chloride 
• 78072-86-3 1-((1S,2R)-2-Chloro-cyclopropyl)-4-(1-chloro-1-methyl-ethyl)-benzene 
• 80857-72-3 trans-1-chloro-2-(4-cinnamoylphenyl)cyclopropane 
• 137601-85-5 p-(trans-2-Chlorocyclopropyl)-α-methylbenzyl Alcohol 
• 78072-81-8 1-((1S,2R)-2-Chloro-cyclopropyl)-4-isopropenyl-benzene 
• 78072-86-3 1-((1S,2S)-2-Chloro-cyclopropyl)-4-(1-chloro-1-methyl-ethyl)-benzene 
• 137601-85-5 p-(cis-2-Chlorocyclopropyl)-α-methylbenzyl Alcohol 

Relevant articles and documents

Substituent effects on the carbon-13 NMR chemical shifts of cyclopropyl carbons in P-substituted(CIS-and trans-2-chlorocyclopropyl)benzenes

Carbon-13 chemical shifts have been measured for the cyclopropyl carbon atoms of twenty one p-substituted (cis- and trans-2-chlorocyclopropyl)benzenes. The substituent induced chemical shifts (SCS) for the trans derivatives are shifted down field by electron-acceptor substituents and upfield by electron-donating substituents (normal SCS). This SCS trend is the same as those observed for the p-substituted cyclopropylbenzenes, while the SCS range is small because of the decreased polarization of C-1-C-2 bonding due to the attached chlorine atom. For the cis derivatives, SCS for C-1 and C-3(CH 2) carbons were also normal, while no measurable SCS was observed for C-2(CCl). The SCS well fitted with the LSFE equation, indicating that the SCS were controlled mainly by a polar effect, except for C-2(CCl, cis).