83719-44-2 Usage
Uses
Used in Medicinal Chemistry and Pharmaceutical Research:
[(5-methylthiophen-2-yl)methylidene]hydrazine is used as a compound in medicinal chemistry and pharmaceutical research for its ability to interact with biological systems. Its unique structure and reactivity allow it to be a promising candidate for the development of new drugs and therapies.
Used in Organic Synthesis:
[(5-methylthiophen-2-yl)methylidene]hydrazine is used as a building block in the synthesis of various organic compounds. Its versatile chemical properties make it a valuable component in creating new materials and compounds for a range of applications in the fields of chemistry and biology.
Used in the Development of New Materials:
The reactivity and chemical properties of [(5-methylthiophen-2-yl)methylidene]hydrazine make it a valuable compound for the development of new materials in the fields of chemistry and biology. Its potential applications in this area are still being explored, but its unique structure and properties offer promising possibilities for future advancements.
Used in Chemical Research:
[(5-methylthiophen-2-yl)methylidene]hydrazine is also used in chemical research to study its properties, reactivity, and potential applications. This research can lead to a better understanding of the compound and its potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 83719-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,7,1 and 9 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83719-44:
(7*8)+(6*3)+(5*7)+(4*1)+(3*9)+(2*4)+(1*4)=152
152 % 10 = 2
So 83719-44-2 is a valid CAS Registry Number.
83719-44-2Relevant academic research and scientific papers
Synthesis and X-ray Photoelectron Spectra of Some Azines
El-Rayyes, Nizar R.,Katrib, Ali H.
, p. 132 - 134 (2007/10/02)
Arylhydrazone-N-carboxylic esters (I) were treated with hydrazine hydrate, or sodium hydroxide, to give the hydrazones (II).Acidification of the latter produced the corresponding azines (III).The structures of compounds I - III were substantiated by chemical and spectral analysis.
