133032-05-0

Basic information

• Product Name: (3-Chloro-phenyl)-(2-fluoro-phenyl)-methanone
• CAS NO: 133032-05-0
• Molecular Weight: 234.657
• Mol File: 133032-05-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3-Chloro-phenyl)-(2-fluoro-phenyl)-methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (3-Chloro-phenyl)-(2-fluoro-phenyl)-methanone(133032-05-0)
• EPA Substance Registry System: (3-Chloro-phenyl)-(2-fluoro-phenyl)-methanone(133032-05-0)

Safety Data

• Hazardous Substances Data: 133032-05-0(Hazardous Substances Data)

Upstream product

• 784-38-3 2-amino-5-chloro-2'-fluorobenzophenone 
• 108-37-2 1-bromo-3-chlorobenzene 
• 446-52-6 2-Fluorobenzaldehyde 
• 133031-89-7 C₁₇H₁₃ClFN₅O₃ 
• 133031-86-4 C₁₇H₁₃Cl₂FN₂O₃ 
• 133031-94-4 C₃₅H₂₈ClFN₃O₃P 
• 109-86-4 2-methoxy-ethanol 

Relevant articles and documents

Elemental step thermodynamics of various analogues of indazolium alkaloids to obtaining hydride in acetonitrile

A series of analogues of indazolium alkaloids were designed and synthesized. The thermodynamic driving forces of the 6 elemental steps for the analogues of indazolium alkaloids to obtain hydride in acetonitrile were determined using an isothermal titration calorimeter (ITC) and electrochemical methods, respectively. The effects of molecular structure and substituents on the thermodynamic driving forces of the 6 steps were examined. Meanwhile, the oxidation mechanism of NADH coenzyme by indazolium alkaloids was examined using the chemical mimic method. The result shows that the oxidation of NADH coenzyme by indazolium alkaloids in vivo takes place by one-step concerted hydride transfer mechanism.