147808-02-4 Usage
Uses
Used in Pharmaceutical Industry:
1,4-DIIODO-2-FLUOROBENZENE is used as a synthetic intermediate for the development of various pharmaceuticals, leveraging its structural properties to create novel drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 1,4-DIIODO-2-FLUOROBENZENE serves as a precursor in the synthesis of compounds designed to protect crops and enhance agricultural productivity, capitalizing on its reactivity and structural features.
Used in Specialty Chemicals:
1,4-DIIODO-2-FLUOROBENZENE is utilized as a component in the production of specialty chemicals, where its unique combination of iodine and fluorine atoms contributes to the creation of high-value chemical products with specific applications.
Used in Dye Manufacturing:
1,4-DIIODO-2-FLUOROBENZENE is also employed in the manufacture of dyes, where its chemical structure imparts color and other properties essential for various industrial and commercial uses.
It is crucial to handle 1,4-DIIODO-2-FLUOROBENZENE with caution due to its potential hazards to human health and the environment, particularly given its insolubility in water and high solubility in organic solvents such as ethanol, ethyl acetate, and acetone.
Check Digit Verification of cas no
The CAS Registry Mumber 147808-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,8,0 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 147808-02:
(8*1)+(7*4)+(6*7)+(5*8)+(4*0)+(3*8)+(2*0)+(1*2)=144
144 % 10 = 4
So 147808-02-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3FI2/c7-5-3-4(8)1-2-6(5)9/h1-3H
147808-02-4Relevant articles and documents
Synthesis of [2]- and [3]rotaxanes through Sonogashira coupling
Giguère, Jean-Beno?t,Thibeault, Dominic,Cronier, Francis,Marois, Jean-Sébastien,Auger, Michèle,Morin, Jean-Fran?ois
supporting information; experimental part, p. 5497 - 5500 (2010/01/03)
The synthesis of new [2]- and [3]rotaxanes through Sonogashira coupling has been accomplished in the aim to built oligo(phenyleneethynylene) (OPE) encircled by crown ethers. Optimization of the Sonogashira coupling for the formation of the [2]rotaxane (ca
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).
