371-89-1 Usage
Haloalkane
A class of organic compounds 1-Chloro-1-fluorocyclohexane is a haloalkane, which means it contains one or more halogen atoms, such as chlorine and fluorine, in its structure.
Cyclohexane ring
The compound's structure The chlorine and fluorine atoms are attached to a cyclohexane ring, which is a six-carbon ring with a specific arrangement of hydrogen atoms.
Intermediate in pharmaceuticals and agrochemicals
Industrial applications 1-Chloro-1-fluorocyclohexane is commonly used as an intermediate in the production of pharmaceuticals and agrochemicals, meaning it is a precursor to other compounds in the synthesis process.
Solvent in organic synthesis
Use in chemical reactions The compound is also used as a solvent in various organic synthesis processes, helping to dissolve and facilitate reactions between other chemicals.
Hazardous chemical
Safety concerns 1-Chloro-1-fluorocyclohexane is considered to be a hazardous chemical, which means it can pose risks to human health and the environment if not handled properly.
Precautions and protective equipment
Safe handling When working with 1-Chloro-1-fluorocyclohexane, it is important to take precautions, such as wearing proper protective equipment (e.g. gloves, goggles, lab coat) and following safety regulations to minimize the risks associated with handling this hazardous compound.
Check Digit Verification of cas no
The CAS Registry Mumber 371-89-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 1 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 371-89:
(5*3)+(4*7)+(3*1)+(2*8)+(1*9)=71
71 % 10 = 1
So 371-89-1 is a valid CAS Registry Number.
371-89-1Relevant articles and documents
Chlorination of oximes in hydrogen fluoride: formation of gem-dihalogenoalkanes
Tordeux, Marc,Boumizane, Khalid,Wakselman, Claude
, p. 207 - 214 (2007/10/02)
The action of chlorine on oximes in hydrogen fluoride as a medium gives gem-dihalogenoalkanes.The reaction proceeds through the intermediate formation of gem-chloronitrosoalkanes.The relative proportions between gem-dichloro, -difluoro and -fluorochloro compounds are dependent on the presence of a cosolvent.The use of other oxidants, such as nitric oxide, dinitrogen tetroxide or nitrosyl chloride, gives similar compounds: - Keywords: Chlorination, Oximes; Hydrogen fluoride; Dihalogenoalkanes; NMR spectroscopy, Mass spectrometry
