914636-20-7 Usage
General Description
4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID is a chemical compound with the molecular formula C8H4F3IO2. It is a white to off-white crystalline powder that is insoluble in water but soluble in organic solvents. 4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID is a derivative of benzoic acid and contains both iodine and trifluoromethyl functional groups, making it useful for a variety of chemical reactions and applications. It is commonly used in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it can be used as a building block in the production of dyes and pigments, and as an intermediate in the synthesis of specialty chemicals. Overall, 4-IODO-3-(TRIFLUOROMETHYL)BENZOIC ACID has widespread applications in the chemical and pharmaceutical industries due to its unique chemical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 914636-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,6,3 and 6 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 914636-20:
(8*9)+(7*1)+(6*4)+(5*6)+(4*3)+(3*6)+(2*2)+(1*0)=167
167 % 10 = 7
So 914636-20-7 is a valid CAS Registry Number.
914636-20-7Relevant articles and documents
Photoinduced Charge-Transfer State of 4-Carbazolyl-3-(trifluoromethyl)benzoic Acid: Photophysical Property and Application to Reduction of Carbon?Halogen Bonds as a Sensitizer
Matsubara, Ryosuke,Shimada, Toshiyuki,Kobori, Yasuhiro,Yabuta, Tatsushi,Osakai, Toshiyuki,Hayashi, Masahiko
, p. 2006 - 2010 (2016/07/28)
The photoinduced persistent intramolecular charge-transfer state of 4-carbazolyl-3-(trifluoromethyl)benzoic acid was confirmed. It showed a higher catalytic activity in terms of yield and selectivity in the photochemical reduction of alkyl halides compared to the parent carbazole. Even unactivated primary alkyl bromides could be reduced by this photocatalyst. The high catalytic activity is rationalized by considering the slower backward single-electron transfer owing to the spatial separation of the donor and acceptor subunits.
COMPOUNDS AND METHODS FOR MODULATING FXR
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Page/Page column 42, (2008/06/13)
Compounds of formula (I) wherein variables are as defined herein and their pharmaceutical compositions and methods of use are disclosed as useful for treating dyslipidemia and related diseases.
