34552-16-4 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-3-FLUORO-5-METHYLPYRIDINE is used as a synthetic intermediate for the development of pharmaceuticals, contributing to the creation of new drugs and medicinal compounds. Its unique structure allows for versatile chemical reactions that can lead to the production of a wide range of therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-BROMO-3-FLUORO-5-METHYLPYRIDINE serves as a key intermediate in the synthesis of various agrochemicals, including pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and weeds, thereby supporting agricultural productivity.
Used in Chemical Research and Development:
2-BROMO-3-FLUORO-5-METHYLPYRIDINE is utilized as a research compound in the field of chemical research and development. It aids scientists in exploring new chemical reactions, understanding molecular interactions, and developing innovative applications for this class of compounds.
Safety Considerations:
Given its flammable nature, 2-BROMO-3-FLUORO-5-METHYLPYRIDINE requires careful handling and storage to mitigate potential health risks. Precautions should be implemented to ensure safe usage and to prevent accidents during its application in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 34552-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34552-16:
(7*3)+(6*4)+(5*5)+(4*5)+(3*2)+(2*1)+(1*6)=104
104 % 10 = 4
So 34552-16-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrFN/c1-4-2-5(8)6(7)9-3-4/h2-3H,1H3
34552-16-4Relevant academic research and scientific papers
Synthesis of Halogenated Pyridines via the CuCl-Catalyzed Addition of Polyhaloacetonitriles to Olefins
Pews, R. Garth,Lysenko, Zenon
, p. 5115 - 5119 (2007/10/02)
Halogenated acetonitriles add smoothly to acrolein, methacrolein, and methacrolein dimethyl acetal in the presence of a catalytic amount of CuCl and triphenylphosphine, tri-n-butylphosphine, or triethylamine to give halogenated difunctional adducts.The adducts have been cyclized in high yields under acidic conditions to halogenated pyridines.