17376-63-5 Usage
Uses
Used in Medicinal Chemistry:
Ethyl 4-amino-1,2,5-oxadiazole-3-carboxylate (SALTDATA: FREE) is used as a key intermediate in the synthesis of new drugs for various therapeutic applications. Its unique structure allows for the creation of molecules with specific biological activities, making it a valuable component in the development of pharmaceuticals.
Used in Chemical Synthesis:
In the field of organic chemistry, Ethyl 4-amino-1,2,5-oxadiazole-3-carboxylate (SALTDATA: FREE) serves as a versatile building block for the creation of complex molecules. Its reactivity and the presence of multiple functional groups facilitate its incorporation into a wide range of chemical structures, enhancing its utility in the synthesis of specialty chemicals and materials.
Used in Research and Development:
Ethyl 4-amino-1,2,5-oxadiazole-3-carboxylate (SALTDATA: FREE) is utilized as a research compound in academic and industrial laboratories. Its properties and reactivity are studied to understand its potential applications and to explore new methods for its synthesis and modification, contributing to the advancement of chemical knowledge and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 17376-63-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,3,7 and 6 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17376-63:
(7*1)+(6*7)+(5*3)+(4*7)+(3*6)+(2*6)+(1*3)=125
125 % 10 = 5
So 17376-63-5 is a valid CAS Registry Number.
17376-63-5Relevant academic research and scientific papers
A Safer Synthesis of the Explosive Precursors 4-Aminofurazan-3-Carboxylic Acid and its Ethyl Ester Derivative
Johnson, Eric C.,Miller, Christopher W.,Orlicki, Joshua A.,Sabatini, Jesse J.,Sausa, Rosario C.
, p. 599 - 603 (2020/04/20)
A safe and efficient one-pot synthesis of 4-aminofurazan-3-carboxylic acid and its hydrogen chloride gas-free conversion to the ethyl ester derivative are described. Previous syntheses of these intermediates were plagued with mischaracterization issues, low yields, and/or dangerous exothermic profiles. The safe scale-up of these materials not only provides benefits to the energetic materials community but may also be of importance to the pharmaceutical and agrochemicals industries.
Reduction of the furoxan ring to the furazan ring in some carbonyl-substituted furoxans
Kulikov, A. S.,Makhova, N. N.,Godovikova, T. I.,Golova, S. P.,Khmel'nitskii, L. I.
, p. 630 - 631 (2007/10/02)
It was shown that the furoxan ring is efficiently reduced to the furazan ring in carboxyl-substituted furoxans with other functional groups by the action of the SnCl2-HCl-AcOH system. - Key words: furazans, furoxans, reduction.
