501433-05-2 Usage
Uses
Used in Organic Synthesis:
4-IODO-2,3-DIFLUOROBENZOIC ACID is used as a key intermediate for the preparation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure allows it to be a versatile building block in the synthesis of a wide range of compounds.
Used in the Synthesis of Novel Materials:
4-IODO-2,3-DIFLUOROBENZOIC ACID is utilized as a precursor in the development of new materials, showcasing its potential in material science for creating innovative substances with specific properties.
Used in Antimicrobial Applications:
4-IODO-2,3-DIFLUOROBENZOIC ACID is used as an antimicrobial agent due to its demonstrated effectiveness against certain microorganisms, making it a candidate for applications in healthcare and related industries where microbial control is essential.
Used in Antifungal Applications:
In the field of antifungal treatments, 4-IODO-2,3-DIFLUOROBENZOIC ACID is employed for its ability to combat fungal infections, highlighting its potential use in agricultural and medical sectors to prevent and treat fungal-related issues.
Check Digit Verification of cas no
The CAS Registry Mumber 501433-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,4,3 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 501433-05:
(8*5)+(7*0)+(6*1)+(5*4)+(4*3)+(3*3)+(2*0)+(1*5)=92
92 % 10 = 2
So 501433-05-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H3F2IO2/c8-5-3(7(11)12)1-2-4(10)6(5)9/h1-2H,(H,11,12)
501433-05-2Relevant academic research and scientific papers
The basicity gradient-driven migration of iodine: Conferring regioflexibility on the substitution of fluoroarenes
Rausis, Thierry,Schlosser, Manfred
, p. 3351 - 3358 (2007/10/03)
Six different fluoroarenes were submitted to the same transformations. Direct deprotonation with alkyllithium or lithium dialkylamide as reagents and subsequent carboxylation afforded the acids 1, 6, 11, 16, 18, and 23. If the aryllithium intermediate was trapped with iodine rather than with dry ice, an iodofluoroarene (2, 7, 12, 17, 19, and 24) was formed. This, upon treatment with lithium diisopropylamide, underwent deprotonation and iodine migration. The resulting new aryllithium species was intercepted either by carboxylation, to give the acids 3, 8, 13, 20, and 25, or by neutralization, to produce the iodofluoroarenes 4, 9, 14, 21, and 26. The latter family of compounds was converted into another set of acids 5, 10, 15, 22, and 27 by subsequent treatment with butyllithium or isopropylmagnesium chloride and carbon dioxide. ( Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002).
