501433-14-3 Usage
Description
Methyl 2,6-Difluoro-3-iodobenzoate is a chemical compound with the molecular formula C8H6F2IO2. It is a fluorinated derivative of benzoic acid and contains both methyl and iodine functional groups. Methyl 2,6-Difluoro-3-iodobenzoate is known for its high reactivity, making it a valuable intermediate in the preparation of fluorinated organic compounds. Due to its unique chemical properties, Methyl 2,6-Difluoro-3-iodobenzoate has potential applications in the development of new drugs and materials.
Uses
Used in Pharmaceutical Industry:
Methyl 2,6-Difluoro-3-iodobenzoate is used as a building block for the synthesis of various pharmaceuticals. Its unique chemical properties and high reactivity make it a valuable intermediate in the development of new drugs.
Used in Agrochemical Industry:
Methyl 2,6-Difluoro-3-iodobenzoate is also used as a building block for the synthesis of agrochemicals. Its reactivity and unique properties contribute to the development of effective and innovative agrochemical products.
Used in Materials Science:
Methyl 2,6-Difluoro-3-iodobenzoate is used in the development of new materials due to its unique chemical properties. Its reactivity and functional groups make it a promising candidate for the creation of advanced materials with specific properties.
It is important to handle Methyl 2,6-Difluoro-3-iodobenzoate with care, as it is a hazardous chemical that may cause irritation and harm to human health and the environment if not properly managed.
Check Digit Verification of cas no
The CAS Registry Mumber 501433-14-3 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, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 501433-14:
(8*5)+(7*0)+(6*1)+(5*4)+(4*3)+(3*3)+(2*1)+(1*4)=93
93 % 10 = 3
So 501433-14-3 is a valid CAS Registry Number.
501433-14-3Relevant articles and documents
Structural modifications of quinolone-3-carboxylic acids with anti-HIV activity
He, Qiu-Qin,Gu, Shuang-Xi,Liu, Jia,Wu, Hai-Qiu,Zhang, Xuan,Yang, Liu-Meng,Zheng, Yong-Tang,Chen, Fen-Er
experimental part, p. 5039 - 5045 (2011/10/03)
A series of new quinolone-3-carboxylic acids featuring a hydroxyl group at C-5 position were synthesized and evaluated for their in vitro activity against HIV in C8166 cell culture. All the compounds showed anti-HIV-1 activity with low micromolar to submi
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).
