40483-47-4 Usage
Description
5-METHYL-1,2,4-OXADIAZOL-3-AMINE is a heterocyclic chemical compound characterized by its molecular formula C3H5N3O. It features an oxadiazole ring with a methyl group attached, which endows it with unique chemical properties. Known for its high thermal stability, this compound serves as a versatile building block in organic synthesis and drug development, with potential applications spanning pharmaceuticals, agrochemicals, and materials science.
Uses
Used in Pharmaceutical Industry:
5-METHYL-1,2,4-OXADIAZOL-3-AMINE is used as a key building block in the synthesis of various pharmaceutical compounds. Its unique structure and properties make it a valuable component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Agrochemical Industry:
In the agrochemical sector, 5-METHYL-1,2,4-OXADIAZOL-3-AMINE is utilized as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its high thermal stability and reactivity contribute to the creation of effective and stable agrochemical products.
Used in Materials Science:
5-METHYL-1,2,4-OXADIAZOL-3-AMINE is employed as a precursor in the development of advanced materials with specific properties, such as high thermal stability, flame retardancy, or chemical resistance. Its incorporation into materials can enhance their performance in various applications, including aerospace, automotive, and electronics industries.
Used in Organic Synthesis:
As a versatile building block, 5-METHYL-1,2,4-OXADIAZOL-3-AMINE is used in organic synthesis for the creation of a wide range of organic compounds. Its unique chemical properties allow for the formation of various functional groups and structures, expanding the scope of synthetic chemistry.
Used in Research Community:
5-METHYL-1,2,4-OXADIAZOL-3-AMINE has garnered attention in the research community due to its potential in various industrial and scientific applications. Researchers are exploring its use in the development of new materials, pharmaceuticals, and agrochemicals, as well as its potential role in advancing scientific understanding of chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 40483-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,8 and 3 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 40483-47:
(7*4)+(6*0)+(5*4)+(4*8)+(3*3)+(2*4)+(1*7)=104
104 % 10 = 4
So 40483-47-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H5N3O/c1-2-5-3(4)6-7-2/h1H3,(H2,4,6)
40483-47-4Relevant articles and documents
PHOTOCHEMICAL BEHAVIOUR OF 1,2,5-OXADIAZOLES - IRRADIATION OF SOME 3-ACYLAMINO-1,2,5-OXADIAZOLES IN THE PRESENCE OF NUCLEOPHILES
Buscemi, Silvestre,Frenna, Vincenzo,Caronna, Tullio,Vivona, Nicolo
, p. 2313 - 2322 (2007/10/02)
The photochemical behaviour of some 3-acylamino-1,2,5-oxadiazoles (furazans) has been investigated.On irradiation at 254 nm in the presence of nucleophiles (ammonia, primary or secondary amines), the photoreaction produced 3-substituted 1,2,3-oxadiazoles in which the substituent at C(3) arises from the used reagent.Some mechanistic considerations are reported.
