20240-99-7 Usage
Uses
Used in Organic Chemistry:
(1E)-1-(2-methoxyphenyl)-3,3-dimethyltriaz-1-ene is utilized as a synthetic intermediate in organic chemistry for the preparation of various compounds. Its unique structure allows for the synthesis of a range of chemical entities, contributing to the development of new materials and pharmaceuticals.
Used in Pharmaceutical Chemistry:
Due to its potential biological activities, (1E)-1-(2-methoxyphenyl)-3,3-dimethyltriaz-1-ene is used as a subject for research in pharmaceutical chemistry. Its exploration may lead to the discovery of new drugs or therapeutic agents, particularly if its biological properties align with desired pharmacological effects.
Used in Agricultural Chemistry:
(1E)-1-(2-methoxyphenyl)-3,3-dimethyltriaz-1-ene may also be of interest in agricultural chemistry, where it could be investigated for applications such as the development of new pesticides, herbicides, or other agrochemicals. Its potential biological activities could be harnessed to improve crop protection or yield.
Check Digit Verification of cas no
The CAS Registry Mumber 20240-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,2,4 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20240-99:
(7*2)+(6*0)+(5*2)+(4*4)+(3*0)+(2*9)+(1*9)=67
67 % 10 = 7
So 20240-99-7 is a valid CAS Registry Number.
20240-99-7Relevant academic research and scientific papers
Highly efficient palladium-catalyzed cross-coupling of diarylborinic acids with arenediazoniums for practical diaryl synthesis
Wang, Fengze,Wang, Chen,Sun, Guoping,Zou, Gang
supporting information, (2019/12/25)
A highly efficient cross-coupling of cost-effective diarylborinic acids with both isolatable and latent arenediazoniums, i.e. tetrafluoroborates and aryltriazenes, respectively, has been developed with a practical palladium catalyst system under base-free conditions in open flask at room temperature. A variety of electronically and sterically various biaryls, in particular, those bearing a coordinative ortho-substituent, could be obtained in good to excellent yields by using 0.3 mol% palladium acetate as catalyst. Features of the protocol including cost-effectiveness of diarylborinic acids, efficacy to heteroatom ortho-substituted substrates and high chemoselectivity to aryl chlorides have been clearly demonstrated in practical synthesis of fungicide Boscalid.
Synthesis in 3 Azafluorene Group. Part-III
Chatterjea, J. N.,Shaw, S. C.,Prasad, Y.,Singh, R. P.
, p. 1028 - 1031 (2007/10/02)
The Hey-Elks route to arylated pyridines has been utilised in the synthesis of 3-azafluorenes.The pyrido-coumarin (23) and the related chromene (24) have been synthesised.
