845866-85-5 Usage
Uses
Used in Pharmaceutical Industry:
3-Fluoro-5-iodo bromobenzene is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Fluoro-5-iodo bromobenzene serves as a key intermediate in the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and food security.
Used in Organic Synthesis:
3-Fluoro-5-iodo bromobenzene is used as a building block in organic synthesis for the creation of a wide range of organic compounds. Its halogenated nature facilitates various chemical reactions, enabling the synthesis of complex molecules with diverse applications in industries such as materials science, polymer chemistry, and specialty chemicals.
Used in Research and Development:
3-Fluoro-5-iodo bromobenzene is employed in research and development as a valuable tool for studying chemical reactions and exploring new synthetic pathways. Its unique properties make it an attractive candidate for investigating novel reaction mechanisms, understanding structure-activity relationships, and developing innovative materials with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 845866-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,5,8,6 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 845866-85:
(8*8)+(7*4)+(6*5)+(5*8)+(4*6)+(3*6)+(2*8)+(1*5)=225
225 % 10 = 5
So 845866-85-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H3BrFI/c7-4-1-5(8)3-6(9)2-4/h1-3H
845866-85-5Relevant articles and documents
Copper-Mediated Fluorination of Aryl Trisiloxanes with Nucleophilic Fluoride
Dorel, Ruth,Boehm, Philip,Schwinger, Daniel P.,Hartwig, John F.
, p. 1759 - 1762 (2020)
A method for the nucleophilic fluorination of heptamethyl aryl trisiloxanes to form fluoroarenes is reported. The reaction proceeds in the presence of Cu(OTf)2 and KHF2 as the fluoride source under mild conditions for a broad range of heptamethyltrisiloxyarenes with high functional group tolerance. The combination of this method with the silylation of aryl C?H bonds enables the regioselective fluorination of non-activated arenes controlled by steric effects following a two-step protocol.
