7144-78-7 Usage
Uses
Used in Organic Synthesis:
[(E)-methyldiazenyl](diphenyl)methyl acetate is used as a reagent for the formation of diazo compounds, which are essential in various chemical reactions and processes. Its unique structure allows it to participate in a range of reactions, making it a valuable asset in the field of organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(E)-methyldiazenyl](diphenyl)methyl acetate serves as a precursor in the synthesis of other organic compounds. Its ability to form diazo compounds contributes to the development of new drugs and pharmaceutical products.
Used in Pesticide Development:
[(E)-methyldiazenyl](diphenyl)methyl acetate has been studied for its potential as a pesticide. Its chemical properties make it a candidate for the development of new and effective pest control solutions.
Used as an Enzyme Inhibitor:
[(E)-methyldiazenyl](diphenyl)methyl acetate has also been investigated for its potential as an inhibitor of certain enzymes. Its ability to interact with enzymes could lead to the development of new treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 7144-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 4 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7144-78:
(6*7)+(5*1)+(4*4)+(3*4)+(2*7)+(1*8)=97
97 % 10 = 7
So 7144-78-7 is a valid CAS Registry Number.
7144-78-7Relevant academic research and scientific papers
Synthetic applications of α-hydroxydiazenes. III. Uncatalyzed and phenol catalyzed hydroalkylation of alkenes and of azobenzene with alkylazodiphenylmethanols
Yeung, Dominic W. K.,Warkentin, John
, p. 2386 - 2394 (2007/10/02)
Alkylazodiphenylmethanols (C6H5)2C(OH)N=NR, (R = CH(CH3)2, CH2CH3, CH3), when decomposed in the presence of olefinic substrates or in the presence of azobenzene, hydroalkylate those substrates.Addition of R and H across the double bond of an unsymmetric alkene occurs with the regiochemistry expected for a radical mechanism, in which the grooup R adds first.Radical intermediates from decomposition of alkylazodiphenylmethanols have been demonstrated earlier with spin trapping experiments.The fact that addition of phenol can enhance the yield of hydroalkylation product suggests that the process is a radical chain reaction, with chain carrying steps consisting of the reactions: (i) R. + CH2=CHY -> RCH2C.HY (ii) RCH2C.HY + (C6H5)2C(OH)N2R -> RCH2CH2Y + (C6H5)2CO + N2 + R..One deuterioalkylation and some yield-optimizing experiments are also reported.
