637-80-9 Usage
Uses
Used in Pharmaceutical Industry:
Ethylhydrazinoacetate is used as a key reactant in the synthesis of various pharmaceuticals for its ability to form heterocyclic compounds, which are essential in the development of new drugs.
Used in Agrochemical Industry:
In the agrochemical sector, ethylhydrazinoacetate is utilized as a reactant in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Chemical Manufacturing:
Ethylhydrazinoacetate is used as a building block in the manufacture of corrosion inhibitors, which are vital for protecting materials from the damaging effects of corrosion.
Used in Dye and Pigment Industry:
ethylhydrazinoacetate is also employed in the production of dyes and pigments, where its chemical properties contribute to the creation of vibrant and stable colorants for various applications.
Used in Therapeutic Applications:
Ethylhydrazinoacetate is studied for its potential therapeutic uses, particularly in the treatment of cancer and neurodegenerative disorders, due to its unique chemical structure and reactivity.
Used in Research and Development:
In research settings, ethylhydrazinoacetate is used as a versatile compound for exploring new chemical reactions and developing innovative applications in various fields, including material science and medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 637-80-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 637-80:
(5*6)+(4*3)+(3*7)+(2*8)+(1*0)=79
79 % 10 = 9
So 637-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C4H10N2O2/c1-2-3(6-5)4(7)8/h3,6H,2,5H2,1H3,(H,7,8)/p-1
637-80-9Relevant academic research and scientific papers
Synthesis and properties of 3-oxo-1,2-diazetidinium ylides
Taylor, Edward C.,Haley, Neil F.,Clemens, Robert J.
, p. 7743 - 7752 (2007/12/18)
Treatment of α-chloroacylhydrazones of diaryl and certain aralkyl and dialkyl ketones with sodium hydride in anhydrous tetrahydrofuran gives 1-(disubstituted methylene)-3-oxo-1,2-diazetidinium inner salts (ylides). The reaction pathway involves formation of the hydrazone anion followed by intramolecular SN2 halide displacement (with complete inversion at the α carbon) by the sp2 imine nitrogen. These 1-(disubstituted methylene)-3-oxo-1,2-diazetidinium ylides are reduced by sodium borohydride to give 1-substituted 1,2-diazetidin-3-ones, undergo dipolar cycloaddition reactions to give fused aza-β-lactams, and can be hydrolyzed with p-toluenesulfonic acid monohydrate to the p-toluenesulfonic acid salt of 1,2-diazetidinone.
