29418-25-5 Usage
Description
(E)-bis(2,4-dimethylphenyl)diazene, with the chemical formula C14H18N2, is a diazene compound characterized by a pair of adjacent nitrogen atoms. Derived from benzene, this compound features two 2,4-dimethylphenyl groups connected to an azene functional group, forming a linear structure. Known for its high reactivity, (E)-bis(2,4-dimethylphenyl)diazene is a compound of interest in organic chemistry, with potential applications in pharmaceuticals and material science.
Uses
Used in Organic Synthesis:
(E)-bis(2,4-dimethylphenyl)diazene is used as a reagent in organic synthesis for its high reactivity, allowing for the creation of various complex organic molecules.
Used in Chemical Reactions:
(E)-bis(2,4-dimethylphenyl)diazene serves as a reagent in chemical reactions, facilitating specific transformations and contributing to the advancement of organic chemistry.
Used in Pharmaceutical Industry:
(E)-bis(2,4-dimethylphenyl)diazene holds potential applications in the pharmaceutical industry, where its unique properties may be harnessed for the development of new drugs and therapies.
Used in Material Science:
In the field of material science, (E)-bis(2,4-dimethylphenyl)diazene may be utilized to develop novel materials with specific properties, such as improved reactivity or stability.
Overall, (E)-bis(2,4-dimethylphenyl)diazene is a versatile compound with a wide range of potential applications across various industries, making it a valuable subject of research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 29418-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,4,1 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 29418-25:
(7*2)+(6*9)+(5*4)+(4*1)+(3*8)+(2*2)+(1*5)=125
125 % 10 = 5
So 29418-25-5 is a valid CAS Registry Number.
29418-25-5Relevant articles and documents
Electrosynthesis of Azobenzenes Directly from Nitrobenzenes
Ma, Yanfeng,Wu, Shanghui,Jiang, Shuxin,Xiao, Fuhong,Deng, Guo-Jun
, p. 3334 - 3338 (2021/10/29)
The electrochemical reduction strategy of nitrobenzenes is developed. The chemistry occurs under ambient conditions. The protocol uses inert electrodes and the solvent, DMSO, plays a dual role as a reducing agent. Its synthetic value has been demonstrated by the highly efficient synthesis of symmetric, unsymmetric and cyclic azo compounds.
Substrate-Controlled Transformation of Azobenzenes to Indazoles and Indoles via Rh(III)-Catalysis
Cai, Shangjun,Lin, Songyun,Yi, Xiangli,Xi, Chanjuan
, p. 512 - 520 (2017/04/26)
Rh(III)-catalyzed substrate-controlled transformation of azobenzenes to indazoles and 2-acyl (NH) indoles is achieved via C-H functionalization. Generally, good functional groups tolerance, satisfying yields, and excellent regio-selectivity are achieved in this reaction. Mechanistically, the reaction with acrylates undergoes β-hydride elimination, while the reaction with vinyl ketones or acrylamides undergoes nucleophilic addition. Copper acetate was supposed to play different roles in the β-hydride elimination to furnish indazoles and nucleophilic addition of C-Rh bond to deliver 2-acyl (NH) indoles.
Iodination of Anilines with Sodium Dichloroiodate
Elmi, Shire,Heggen, Per,Holmelid, Bjarte,Malthe-S?rensen, Didrik,Sydnes, Leiv K.
, p. 385 - 392 (2016/09/14)
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