54210-22-9 Usage
Uses
Used in Organic Synthesis:
(E)-1-(4-butylphenyl)-2-phenyldiazene is used as a reagent in organic synthesis for its ability to participate in various chemical reactions. Its diazene functional group allows for a range of reactions, making it a versatile compound in the field of organic chemistry.
Used in Chemical Reactions:
In the realm of chemical reactions, (E)-1-(4-butylphenyl)-2-phenyldiazene is used as a reagent due to its reactivity under certain conditions. This property makes it valuable for initiating or facilitating specific chemical transformations, contributing to the advancement of chemical research and development.
Used in Research and Development:
(E)-1-(4-butylphenyl)-2-phenyldiazene is also utilized in research and development as a compound that can be further studied and modified to create new materials or improve existing ones. Its unique properties and reactivity make it a promising candidate for the development of novel chemical processes and products.
Used in Pharmaceutical Industry:
While not explicitly mentioned in the provided materials, due to its use in organic synthesis and chemical reactions, (E)-1-(4-butylphenyl)-2-phenyldiazene may also find applications in the pharmaceutical industry. It could potentially be used in the development of new drugs or the improvement of drug synthesis processes.
Check Digit Verification of cas no
The CAS Registry Mumber 54210-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,1 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 54210-22:
(7*5)+(6*4)+(5*2)+(4*1)+(3*0)+(2*2)+(1*2)=79
79 % 10 = 9
So 54210-22-9 is a valid CAS Registry Number.
54210-22-9Relevant academic research and scientific papers
Bouillon, Marc E.,Meyer, Hartmut H.
, p. 3151 - 3161 (2016)
When treated with dilute inorganic acids N,N′-diarylhydrazines (hydrazobenzenes) with an alkyl substituent in the 4-position undergo [5,5]-sigmatropic rearrangement reactions to furnish 4-(4′-aminophenyl)-4-alkylcyclohexa-2,5-dienimines (ipso-benzidines) in moderate to excellent yields. Steric bulk of the 4-alkyl substituent in the starting material decreases the yield of the respective ipso-benzidine. Additional electron-donating alkyl substituents in the ortho- and/or meta-positions on both rings generally promote the reaction and consequently increase the yield of the 4.4′-benzidine rearrangement product. Described herein are our findings regarding the scope and limits of this unusual benzidine rearrangement.
