6589-37-3 Usage
Description
3-tert-butyl-6-methyluracil, also known as 3-tert-butyl-6-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione, is an organic compound with the chemical formula C10H14N2O2. It is a white crystalline solid and is an intermediate in the synthesis of various chemical compounds.
Uses
Used in Chemical Synthesis:
3-tert-butyl-6-methyluracil is used as an intermediate in the synthesis of 3-tert-Butyl-5-chloro-6-hydroxymethyluracil (B997095), a metabolite of Terbacil herbicides. This metabolite is found in plants, animal tissues, and soil, and is used for controlling broadleaf and grassy weeds in various crops.
Used in Pesticide Industry:
3-tert-butyl-6-methyluracil is used as a key intermediate in the production of Terbacil herbicides, which are widely used in agriculture to control weeds and improve crop yield. The herbicides containing this compound are effective against a broad spectrum of weeds, making them valuable in the pesticide industry.
Used in Environmental Research:
As a metabolite of Terbacil herbicides, 3-tert-butyl-6-methyluracil is also used in environmental research to study the fate and behavior of these herbicides in the environment. This helps in understanding their impact on soil, water, and plant life, and aids in the development of safer and more effective herbicides.
Check Digit Verification of cas no
The CAS Registry Mumber 6589-37-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,8 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6589-37:
(6*6)+(5*5)+(4*8)+(3*9)+(2*3)+(1*7)=133
133 % 10 = 3
So 6589-37-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H14N2O2/c1-6-5-7(12)11(8(13)10-6)9(2,3)4/h5H,1-4H3,(H,10,13)
6589-37-3Relevant articles and documents
Preparation method of herbicide 3-tert-butyl-5-chloro-6-methyluracil
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Paragraph 0010; 0028-0031, (2019/05/02)
The invention discloses a preparation method of herbicide 3-tert-butyl-5-chloro-6-methyluracil. The method comprises the steps that a compound acetoacetic ester is taken as a raw material to react with an ammonia source to generate 3-amino-2-butenoic acid ethyl ester, the 3-amino-2-butenoic acid ethyl ester is reacted with tert-butylisocyanate to generate an intermediate, and the 3-tert-butyl-5-chloro-6-methyluracil is obtained after chlorination is conducted on the intermediate. The method has the advantages that the obtaining of the raw material is easy, the technology is brief, the method is economical and environmentally friendly, and the method is suitable for industrial production.