6945-82-0 Usage
Uses
Used in Pesticide Industry:
1-(2,4-dinitrophenoxy)-2-methoxy-4-methylbenzene is used as an active ingredient in pesticides for its ability to effectively inhibit the growth of unwanted plants. Its application in this industry is due to its potent biocidal properties, which help control and eliminate various types of weeds and pests that can damage crops and gardens.
Used in Herbicide Industry:
In the herbicide industry, 1-(2,4-dinitrophenoxy)-2-methoxy-4-methylbenzene is used as a selective agent to control the growth of specific plant species, thereby promoting the growth of desired vegetation. Its targeted action makes it a valuable tool in agricultural practices to maintain a balanced and productive ecosystem.
Used as an Intermediate in Organic Synthesis:
1-(2,4-dinitrophenoxy)-2-methoxy-4-methylbenzene also serves as an intermediate in the synthesis of other organic compounds. Its unique chemical structure allows for further modification and incorporation into a variety of products, contributing to its versatility in the chemical industry.
Safety Precautions:
Given the toxic nature of 1-(2,4-dinitrophenoxy)-2-methoxy-4-methylbenzene, it is crucial to handle this chemical with extreme caution. Proper safety measures, including the use of personal protective equipment and adherence to guidelines for safe storage and disposal, must be followed to minimize the risk of harm to humans and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 6945-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6945-82:
(6*6)+(5*9)+(4*4)+(3*5)+(2*8)+(1*2)=130
130 % 10 = 0
So 6945-82-0 is a valid CAS Registry Number.
6945-82-0Relevant academic research and scientific papers
P(i-BuNCH2CH2)3N: An efficient promoter for the nucleophilic aromatic substitution reaction of aryl fluorides with aryl TBDMS (or TMS) ethers
Urgaonkar, Sameer,Verkade, John G.
, p. 3319 - 3322 (2007/10/03)
(Chemical Equation Presented) The nucleophilic aromatic substitution reaction between electron-deficient aryl fluorides and aryl TBDMS (or TMS) ethers has been shown to be efficiently promoted by proazaphosphatranes such as P(i-BuNCH2CH2)3N (3). Excellent yields of diaryl ether products were obtained under unusually mild conditions.
