145486-55-1 Usage
Family
Biphenyl
It belongs to the biphenyl family of chemical compounds.
Structural features
Methyl and trifluoromethyl groups
The compound contains a methyl group (-CH3) and a trifluoromethyl group (-CF3) in its structure.
Usage
Building block in synthesis
It is often used as a building block in the synthesis of various organic compounds and pharmaceuticals.
Industrial applications
Polymers, plastics, and organic materials
It has a variety of industrial applications, including the production of polymers, plastics, and other organic materials.
Research and development
Creation of new chemical compounds
It is used in research and development for the creation of new chemical compounds with specific properties and applications.
Stability
Relatively stable
The compound is considered to be relatively stable, making it suitable for various applications.
Toxicity
Low toxicity
It has low toxicity, which contributes to its versatility and usefulness in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 145486-55-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,4,8 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 145486-55:
(8*1)+(7*4)+(6*5)+(5*4)+(4*8)+(3*6)+(2*5)+(1*5)=151
151 % 10 = 1
So 145486-55-1 is a valid CAS Registry Number.
145486-55-1Relevant academic research and scientific papers
Nickel/magnesium-lanthanum mixed oxide catalyst in the Kumada-coupling
Kiss, Arpad,Hell, Zoltan,Balint, Maria
experimental part, p. 331 - 335 (2010/02/16)
A new, heterogeneous, magnesium-lanthanum mixed oxide solid base-supported nickel(ii) catalyst was developed. The catalyst was used successfully in the Kumada coupling of aryl halides, especially aryl bromides. The optimal reaction conditions of the coupling were determined.
Structure-reactivity relationships in negishi cross-coupling reactions
Dong, Zhi-Bing,Manolikakes, Georg,Shi, Lei,Knochel, Paul,Mayr, Herbert
supporting information; experimental part, p. 248 - 253 (2010/03/30)
Competition experiments have been performed to determine the relative reactivities of substituted bromobenzenes and of different arylzinc reagents in the [Pd(PPh3)4]-catalyzed Negishi cross-coupling reaction in THF at 25 °C. The crosscoupling reactions are accelerated by electron acceptors in the bromobenzenes, the effect of which increases in the order ortho a larger effect than substituent variations in the arylzinc halides (ρ = -0.98).
