169468-83-1 Usage
General Description
2-Chloro-3,4-difluoronitrobenzene is a specific type of organic compound from the family of nitrobenzenes. It is also known by its systematic name, 1-chloro-2,3-difluoro-4-nitrobenzene. The molecular structure contains a benzene ring, which is a hexagonal ring of six carbon atoms, with attached chlorine, fluorine, and nitro functional groups. The molecular formula of this substance is C6H2ClF2NO2. In terms of its physical properties, there is scant information available as it is characteristic for such specific and niche chemicals. Having similar compounds as a point of reference, it can be inferred that it might be a coloreless liquid or solid with a certain odor, and could hold potential reactivity with other compounds. Its primary usage is likely in the realm of scientific research, particularly synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 169468-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,9,4,6 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 169468-83:
(8*1)+(7*6)+(6*9)+(5*4)+(4*6)+(3*8)+(2*8)+(1*3)=191
191 % 10 = 1
So 169468-83-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H2ClF2NO2/c7-5-4(10(11)12)2-1-3(8)6(5)9/h1-2H
169468-83-1Relevant articles and documents
Synthesis of fluorinated halonitrobenzenes and halonitrophenols using tetrafluoroethylene and buta-1,3-dienes as starting building blocks
Lipkind, M. B.,Nefedov, O. M.,Volchkov, N. V.
, p. 2156 - 2163 (2022/01/22)
The gas-phase copyrolysis of tetrafluoroethylene with buta-1,3-diene in a flow reactor at 495–505 °C produces 3,3,4,4-tetrafluorocyclohex-1-ene, which selectively converted to 1,2-difluorobenzene or 1-chloro-2,3-difluorobenzene. The latter can be converted to 2-chloro-3,4-difluoronitrobenzene, 2,3,4-trifluoronitrobenzene, 2,3-difluoro-6-nitrophenol, or 2-chloro-3-fluoro-4-nitrophenol via nitration, fluorodechlorination, and hydrolysis reactions.
