24336-73-0 Usage
Uses
Used in Organic Synthesis:
2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde is used as a building block in the production of pharmaceuticals and agrochemicals. Its unique structure and properties make it a valuable intermediate in the synthesis of various organic compounds.
Used in Dye and Pigment Production:
2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde is used as a precursor in the manufacture of dyes and pigments. Its fluorinated structure contributes to the development of novel colorants with improved properties.
Used in Fluorinated Organic Compounds:
2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde is used as a starting material in the creation of fluorinated organic compounds. The presence of fluorine atoms in its structure allows for the development of new compounds with enhanced properties.
Used in Fluorinated Polymer and Material Production:
2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde has been studied for its potential use as a precursor in the production of fluorinated polymers and materials. Its unique structure and properties make it a promising candidate for the development of advanced materials with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 24336-73-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,3 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24336-73:
(7*2)+(6*4)+(5*3)+(4*3)+(3*6)+(2*7)+(1*3)=100
100 % 10 = 0
So 24336-73-0 is a valid CAS Registry Number.
24336-73-0Relevant academic research and scientific papers
Expanded porphyrin-like structures based on twinned triphenylenes
Gopee, Hemant,Kong, Xiangfei,He, Zhiqun,Chambrier, Isabelle,Hughes, David L.,Tizzard, Graham J.,Coles, Simon J.,Cammidge, Andrew N.
, p. 9505 - 9511 (2013/10/08)
Triphenylene twins are intriguing structures, and those bridged through their 3,6-positions by dipyrromethene units give a new class of macrocycles that can be viewed as rigid, expanded porphyrin derivatives in which coplanarity is enforced in a formally antiaromatic π system. Somewhat surprisingly, however, macrocyclization leads to significant overall stabilization of the dipyrromethene chromophores.
