7402-79-1 Usage
Description
(2E)-1-(2,4-dinitrophenyl)-2-[1-(4-nitrophenyl)ethylidene]hydrazine is a hydrazone derivative with a molecular formula of C14H10N6O6. It is characterized by the presence of dinitrophenyl and nitrophenyl groups. This chemical compound has potential applications in various fields, including organic synthesis, medicinal chemistry, and as a reagent for detecting certain chemical groups. Its structure and properties make it of interest to researchers in the scientific community.
Uses
Used in Organic Synthesis:
(2E)-1-(2,4-dinitrophenyl)-2-[1-(4-nitrophenyl)ethylidene]hydrazine is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows for versatile reactions and transformations, making it a valuable building block in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2E)-1-(2,4-dinitrophenyl)-2-[1-(4-nitrophenyl)ethylidene]hydrazine is used as a potential lead compound for the development of new pharmaceutical agents. Its chemical properties and reactivity can be exploited to design and synthesize novel drug candidates with potential therapeutic applications.
Used as a Reagent for Detecting Chemical Groups:
(2E)-1-(2,4-dinitrophenyl)-2-[1-(4-nitrophenyl)ethylidene]hydrazine is used as a reagent for detecting specific chemical groups in various chemical and biochemical assays. Its characteristic reactivity and selectivity make it a useful tool for identifying and characterizing different functional groups in complex mixtures.
Used in Pharmacology:
(2E)-1-(2,4-dinitrophenyl)-2-[1-(4-nitrophenyl)ethylidene]hydrazine has been studied for its potential role in pharmacology. Its biological activities and interactions with biological targets make it a promising candidate for further research and development as a therapeutic agent.
Used in Research:
In the research community, (2E)-1-(2,4-dinitrophenyl)-2-[1-(4-nitrophenyl)ethylidene]hydrazine is used as a model compound to study various chemical reactions and processes. Its unique structure and properties provide valuable insights into the mechanisms and dynamics of chemical transformations, contributing to the advancement of scientific knowledge in various disciplines.
Check Digit Verification of cas no
The CAS Registry Mumber 7402-79-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7402-79:
(6*7)+(5*4)+(4*0)+(3*2)+(2*7)+(1*9)=91
91 % 10 = 1
So 7402-79-1 is a valid CAS Registry Number.
7402-79-1Relevant articles and documents
Efficient and highly aldehyde selective wacker oxidation
Teo, Peili,Wickens, Zachary K.,Dong, Guangbin,Grubbs, Robert H.
supporting information; experimental part, p. 3237 - 3239 (2012/08/27)
A method for efficient and aldehyde-selective Wacker oxidation of aryl-substituted olefins using PdCl2(MeCN)2, 1,4-benzoquinone, and t-BuOH in air is described. Up to a 96% yield of aldehyde can be obtained, and up to 99% selectivity can be achieved with styrene-related substrates.
