439692-54-3 Usage
General Description
6-TERT-BUTYL-3H-THIENO[2,3-D]PYRIMIDIN-4-ONE, also known as terbuthylazine, is a chemical compound primarily used as an herbicide. It belongs to the thiazine chemical class and is used to control a broad spectrum of weeds in a variety of crops. Terbuthylazine works by inhibiting photosynthesis in the target plants, leading to their eventual death. It is known for its effectiveness in controlling annual grasses and broadleaf weeds and is often formulated as a water-dispersible granule for application in agriculture. However, it is also important to note that terbuthylazine has been subject to controversy and regulatory scrutiny due to concerns about its potential impact on human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 439692-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,9,6,9 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 439692-54:
(8*4)+(7*3)+(6*9)+(5*6)+(4*9)+(3*2)+(2*5)+(1*4)=193
193 % 10 = 3
So 439692-54-3 is a valid CAS Registry Number.
439692-54-3Relevant articles and documents
Thiophene [2, 3 - d] pyrimidine derivatives, their preparation and use thereof
-
Paragraph 0128; 0129, (2017/02/17)
The invention provides a thiophene [2, 3-d] pyrimidine derivative containing isoxazole heterocycle shown by formula (I) or a pharmaceutically accepted salt thereof, wherein R1 and R2 are respectively selected from hydrogen, C1-6 alkyl, C1-6 alkoxy, haloge
Discovery of novel thieno[2,3-d]pyrimidin-4-yl hydrazone-based inhibitors of Cyclin D1-CDK4: Synthesis, biological evaluation and structure-activity relationships. Part 2
Horiuchi, Takao,Nagata, Motoko,Kitagawa, Mayumi,Akahane, Kouichi,Uoto, Kouichi
experimental part, p. 7850 - 7860 (2010/04/02)
The design, synthesis and evaluation of novel thieno[2,3-d]pyrimidin-4-yl hydrazone analogues as cyclin-dependent kinase 4 (CDK4) inhibitor are described. Focusing on the optimization of the heteroaryl moiety at the hydrazone with substituted phenyl group