1478-08-6 Usage
Structure
Substituted aromatic compound
Explanation
The compound is derived from a benzene ring, which is an aromatic compound, with additional substituents (atoms or groups of atoms) attached to it.
Explanation
The benzene ring has four fluorine atoms, one iodine atom, and a trifluoromethyl group (CF3) attached to it, which are the substituents that make 1,2,3,4-tetrafluoro-5-iodo-6-(trifluoromethyl)benzene unique.
Explanation
The compound can be used in the development of new pharmaceuticals or advanced materials due to its unique structure and properties.
Explanation
Due to its reactivity and potential toxicity, it is important to handle this chemical with care to minimize risks to human health and the environment.
Explanation
The compound may have toxic effects on living organisms, which is a concern when handling and using it in various applications.
Explanation
Proper handling, storage, and disposal procedures should be followed to minimize the risk of exposure and potential harm to human health and the environment.
Substituents
Four fluorine atoms, one iodine atom, and a trifluoromethyl group
Potential applications
Organic synthesis and materials science
Reactivity
May pose hazards to human health and the environment
Hazardous properties
Potential toxicity
Precautions
Handle with care
Check Digit Verification of cas no
The CAS Registry Mumber 1478-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,7 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1478-08:
(6*1)+(5*4)+(4*7)+(3*8)+(2*0)+(1*8)=86
86 % 10 = 6
So 1478-08-6 is a valid CAS Registry Number.
1478-08-6Relevant academic research and scientific papers
Opening of the four-membered ring in perfluorinated 1-alkyl-2-phenyl-and 1-aryl-1,2-dihydrocyclobutabenzenes in the system I2-SbF5
Mezhenkova,Karpov,Platonov
experimental part, p. 1026 - 1034 (2011/10/19)
Reactions of perfluorinated 1-phenyl-, 1-(2-ethylphenyl)-, 1-(4-ethylphenyl)-, 1-methyl-2-phenyl-, and 1-ethyl-2-phenyl-1,2- dihydrocyclobutabenzenes with iodine in antimony pentafluoride at 130°C, followed by hydroysis of the reaction mixture, resulted in the formation of perfluorinated 2-methyl-, 2-ethyl-2′-methyl-, 4-ethyl-2'-methyl-, 2-ethyl-, and 2-propylbenzophenones via opening of the four-membered ring in the initial cyclobutabenzene at the C1-C2 bond. The presence of hydrogen fluoride facilitates the process and promotes profound transformations leading to anthracene derivatives.
