16879-40-6 Usage
Description
4,6-Dimethyl-2-iodopyrimidine is a chemical compound characterized by the molecular formula C6H7IN2. It is a pyrimidine derivative featuring two methyl groups and an iodine atom, known for its solid state at room temperature and a coloration that ranges from white to yellow. 4,6-Dimethyl-2-iodopyrimidine is notable for its applications in various chemical syntheses and should be handled with caution due to its potential harmful effects if ingested, inhaled, or if it comes into contact with the skin or eyes.
Uses
Used in Pharmaceutical Industry:
4,6-Dimethyl-2-iodopyrimidine serves as a crucial intermediate in the synthesis of various pharmaceuticals. Its unique structure contributes to the development of new drugs, making it an essential component in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4,6-Dimethyl-2-iodopyrimidine is utilized as an intermediate in the production of pesticides and other agrochemicals, highlighting its versatility in chemical synthesis for different applications.
Used in Dye Production:
4,6-Dimethyl-2-iodopyrimidine is also employed in the manufacturing process of dyes, capitalizing on its chemical properties to create a range of colorants used in various industries.
Used in Organic Compounds Synthesis:
Beyond its applications in pharmaceuticals, agrochemicals, and dyes, 4,6-Dimethyl-2-iodopyrimidine is a valuable precursor in the synthesis of other organic compounds, demonstrating its broad utility in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 16879-40-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,7 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16879-40:
(7*1)+(6*6)+(5*8)+(4*7)+(3*9)+(2*4)+(1*0)=146
146 % 10 = 6
So 16879-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H7IN2/c1-4-3-5(2)9-6(7)8-4/h3H,1-2H3
16879-40-6Relevant articles and documents
Improved synthesis of 2,2′-bipyrimidine
Vlad, Gabor,Horvath, Istvan T.
, p. 6550 - 6552 (2002)
A high-yield synthesis was developed for the preparation of 2,2′-bipyrimidine (1) using the Ullmann coupling of 2-iodopyrimidine. The new procedure was also used for the preparation of 4,4′,6,6′-tetramethyl-2,2′-bipyrimidine (2) and 5,5′-dibromo-2,2′-bipyrimidine (3).