89466-39-7 Usage
Uses
Used in Pharmaceutical Industry:
2-Methyl-4-chlor-6-methoxy-pyrimidin is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic properties. Its unique structural features make it a valuable component in the creation of diverse medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Methyl-4-chlor-6-methoxy-pyrimidin serves as an intermediate, playing a crucial role in the synthesis of agrochemicals designed to protect crops and enhance agricultural productivity. Its reactivity and structural attributes are harnessed to develop effective and targeted agrochemical products.
Used in Organic Chemistry:
2-Methyl-4-chlor-6-methoxy-pyrimidin is utilized as a building block in organic chemistry for the production of various heterocyclic compounds. Its presence in these compounds can influence their chemical properties and potential applications, making it an essential component in the synthesis of a wide range of organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 89466-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,6 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89466-39:
(7*8)+(6*9)+(5*4)+(4*6)+(3*6)+(2*3)+(1*9)=187
187 % 10 = 7
So 89466-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H7ClN2O/c1-4-8-5(7)3-6(9-4)10-2/h3H,1-2H3
89466-39-7Relevant articles and documents
Dimethoxypyrimidines as Novel Herbicides. Part 1. Synthesis and Herbicidal Activity of Dimethoxyphenoxypyrimidines and Analogues
Nezu, Yukio,Miyazaki, Masahiro,Sugiyama, Kazuhiko,Kajiwara, Ikuo
, p. 103 - 114 (2007/10/03)
A number of 6-(4-phenoxyphenoxy)pyrimidines and triazines were synthesized and their herbicidal activity was measured. Compounds with the methoxy groups at the 2- and 4-positions on the pyrimidine and triazine rings exhibited high herbicidal activity. Introduction of a substituent into the 5-position of the pyrimidine ring diminished the activity. In the phenoxyphenoxy substructure at the 6-position, the central ether bond can be replaced by a methylene group without loss of activity. The optimum substituent on the terminal phenyl ring was 3-trifluoromethyl. The compounds showed a strong Hill reaction inhibition, but unfortunately showed poor selectivity between weeds and crops. - Keywords: phenoxyphenoxypyrimidines; phenoxyphenoxy-s-triazines; Hill reaction inhibitors; 2,6-dimethoxy-4-pyrimidine; 2,6-dimethoxy-4--s-triazine; herbicides
