4472-45-1 Usage
Description
4-Chloro-2,6-dimethylpyrimidine is a pyrimidine derivative featuring a chlorine atom at the 4-position and two methyl groups at the 2 and 6 positions. It is a versatile chemical compound used in various industrial applications and organic synthesis.
Uses
Used in Pharmaceutical Industry:
4-Chloro-2,6-dimethylpyrimidine is used as a key intermediate for the synthesis of various drugs, including antiviral and antifungal agents. Its unique structure allows for the development of new pharmaceutical compounds with enhanced therapeutic properties.
Used in Agrochemical Production:
4-CHLORO-2,6-DIMETHYLPYRIMIDINE serves as a building block in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals that protect crops and enhance yield.
Used in Dye Manufacturing:
4-Chloro-2,6-dimethylpyrimidine is utilized in the synthesis of dyes, providing a range of color options for various industries, including textiles, plastics, and printing.
Used in Fine Chemicals Industry:
As a versatile intermediate, 4-Chloro-2,6-dimethylpyrimidine is employed in the production of other fine chemicals, expanding its applications across different sectors.
Used in Organic Synthesis:
4-Chloro-2,6-dimethylpyrimidine acts as a precursor for the modification of other molecules, enabling the creation of new chemical compounds with diverse properties and applications in research and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 4472-45-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,7 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4472-45:
(6*4)+(5*4)+(4*7)+(3*2)+(2*4)+(1*5)=91
91 % 10 = 1
So 4472-45-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2/c1-4-3-6(7)9-5(2)8-4/h3H,1-2H3
4472-45-1Relevant articles and documents
Reactions of Halogenomethanes in the Vapor Phase. Part 4. The Reactions of Imidazoles with Chloroform at 550 deg C, and a Comparison with their Liquid-phase Reactions with Trichloroacetate Ion or Hexachloroacetone and Base
Busby, Reginald E.,Khan, Mohammad A.,Khan, Mohammad R.,Parrick, John,Shaw, C. J. Granville,Iqbal, Mohammad
, p. 1427 - 1430 (2007/10/02)
1-Unsubstituted imidazoles and chloroform at 550 deg C in a flow system give mainly 5-chloropyrimidines, together with 4-chloropyrimidines and chloropyrazines.The effects of methyl substituents on the ratio of products is considered.The liquid-phase reactions of 2-methyl- and 2,4,5-trimethyl-imidazole under conditions in which dichlorocarbene is said to be formed in basic or neutral conditions were studied, and compared with the gas-phase reactions with chloroform.
