78350-48-8 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Methoxy-1,2,5-oxadiazol-3-ylamine is used as a key intermediate in the synthesis of various pharmaceutical compounds due to its versatile chemical structure and potential biological activities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Methoxy-1,2,5-oxadiazol-3-ylamine is utilized as a building block for the development of new drugs, leveraging its antimicrobial and anticancer properties to create effective therapeutic agents.
Used in Antimicrobial Applications:
4-Methoxy-1,2,5-oxadiazol-3-ylamine is employed as an antimicrobial agent, contributing to the development of treatments for infections caused by various microorganisms.
Used in Anticancer Research:
4-METHOXY-1,2,5-OXADIAZOL-3-YLAMINE is used in anticancer research for its potential to inhibit the growth of cancer cells, making it a valuable tool in the discovery of new cancer therapies.
Used in Agrochemical Production:
4-Methoxy-1,2,5-oxadiazol-3-ylamine is used as a component in the production of agrochemicals, where its properties may contribute to the development of effective pesticides or herbicides.
Used in Dye Manufacturing:
In the dye industry, 4-Methoxy-1,2,5-oxadiazol-3-ylamine is utilized in the manufacturing process to create dyes with specific color properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 78350-48-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,3,5 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78350-48:
(7*7)+(6*8)+(5*3)+(4*5)+(3*0)+(2*4)+(1*8)=148
148 % 10 = 8
So 78350-48-8 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N3O2/c1-7-3-2(4)5-8-6-3/h1H3,(H2,4,5)
78350-48-8Relevant articles and documents
Nucleophilic substitution in the furazan series. Reactions with O-nucleophiles
Sheremetev,Kharitonova,Mantseva,Kulagina,Shatunova,Aleksandrova,Mel'nikova,Ivanova,Dmitriev,Eman,Yudin,Kuz'min,Strelenko,Novikova,Lebedev,Khmel'nitskii
, p. 1525 - 1537 (2007/10/03)
A number of hydroxy-, alkoxy-, and phenoxyfurazans and difurazanyl ether derivatives were synthesized by reactions of mono-and dinitrofurazans with O-nucleophiles. The effect of the furazan nature and reactant ratio on the structure of products is discussed.