629645-55-2 Usage
General Description
(4-Chloro-2-pyrimidinyl)carbamic acid 1,1-dimethylethyl ester is a chemical compound with the molecular formula C8H11ClN2O2. It is commonly used as a pesticide and herbicide to control various types of weeds, including those in rice paddies, wheat fields, and soybean crops. (4-Chloro-2-pyrimidinyl)carbamic acid 1,1-dimethylethyl ester works by inhibiting the enzyme acetyl-CoA carboxylase, which is essential for fatty acid synthesis in plants, ultimately leading to their death. It is important to handle this chemical with care, as it is toxic to aquatic organisms and may have harmful effects on human health if not properly managed. Additionally, it is important to follow all safety guidelines and regulations when using this compound in agricultural settings.
Check Digit Verification of cas no
The CAS Registry Mumber 629645-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,9,6,4 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 629645-55:
(8*6)+(7*2)+(6*9)+(5*6)+(4*4)+(3*5)+(2*5)+(1*5)=192
192 % 10 = 2
So 629645-55-2 is a valid CAS Registry Number.
629645-55-2Relevant articles and documents
ANTI-ANGIOGENESIS COMPOUND, INTERMEDIATE AND USE THEREOF
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Paragraph 0081; 0083, (2016/04/10)
Disclosed are an anti-abnormal proliferation of angiogenesis compound represented by formula I, use and intermediate thereof. The compound has good effect against abnormal proliferation of angiogenesis, and the activity of the compound is produced by inhibiting VEGFR2. The compound can be used for treating diseases, such as wet macular degeneration, inflammation, malignant tumor and the like, caused by abnormity of angiogenesis and protein kinases such as VEGFR2, FGFR2 and the like.
Synthesis of 2-(pyrimidin-4-yl)indoles
Franco, Laura Hernandez,Palermo, Jorge Alejandro
, p. 975 - 977 (2007/10/03)
The synthesis of 2-substituted isomers of the meridianins, a familiy of bioactive indole alkaloids isolated from the tunicate Aplidium meridianum, was undertaken. The synthetic route comprises six steps, with a microwave promoted Fischer cyclization as th