944707-38-4 Usage
Description
2-Bromo-3-(bromomethyl)-6-methylpyridine is a pyridine derivative with the molecular formula C7H7Br2N. It features a pyridine ring with two bromine atoms and a methyl group attached, making it a valuable building block in the synthesis of various organic compounds.
Uses
Used in Pharmaceutical Industry:
2-Bromo-3-(bromomethyl)-6-methylpyridine serves as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-3-(bromomethyl)-6-methylpyridine is utilized as a precursor in the production of agrochemicals. Its incorporation into these compounds can lead to the creation of effective pesticides and other agricultural products.
Used in Chemical Manufacturing:
2-Bromo-3-(bromomethyl)-6-methylpyridine also plays a role in the broader chemical manufacturing industry. Its reactive bromine and methyl groups make it a versatile intermediate for synthesizing a wide range of organic compounds used in various applications.
Safety Note:
Due to the reactive nature of 2-Bromo-3-(bromomethyl)-6-methylpyridine, it is crucial to handle this compound with care and adhere to proper safety protocols to ensure the well-being of individuals and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 944707-38-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,4,7,0 and 7 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 944707-38:
(8*9)+(7*4)+(6*4)+(5*7)+(4*0)+(3*7)+(2*3)+(1*8)=194
194 % 10 = 4
So 944707-38-4 is a valid CAS Registry Number.
944707-38-4Relevant articles and documents
A new approach to the 1,10-phenanthroline core
Chelucci, Giorgio,Addis, Daniele,Baldino, Salvatore
, p. 3359 - 3362 (2007)
A protocol for the synthesis of substituted 1,10-phenanthrolines is reported. The phenanthroline scaffold has been obtained constructing the central cycle starting from two pyridine rings. The method is hinged upon the intramolecular coupling of cis-1,2-di(2-bromo-3-pyridyl)ethenes that are in turn obtained from the Wittig reaction of 2-bromonicotinaldehydes with phosphonium salts prepared from 2-bromo-3-(bromomethyl)pyridines. Yields up to 75% have been obtained.
