3-methyl-1,2,4-oxadiazole-5-carbaldehyde


Chemical Name: 3-methyl-1,2,4-oxadiazole-5-carbaldehyde
CAS Number: 944906-02-9
Product Number: AG00IIA9(AGN-PC-034NE0)
Synonyms:
MDL No:
Molecular Formula: C4H4N2O2
Molecular Weight: 112.08676

Identification/Properties


Safety Information


GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


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Chemical Structure



3-Methyl-1,2,4-oxadiazole-5-carbaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis for its unique properties. In the field of organic chemistry, this compound is utilized as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals.One of the primary applications of 3-Methyl-1,2,4-oxadiazole-5-carbaldehyde is its role as a precursor in the synthesis of heterocyclic compounds. Its ability to undergo various chemical reactions, such as condensation, oxidation, and reduction, makes it a valuable starting material for the preparation of diverse molecular structures.Furthermore, this compound serves as a valuable intermediate in the synthesis of biologically active molecules due to its pharmacophoric properties. By introducing functional groups onto the oxadiazole ring, chemists can modulate the compound's biological activity, making it a crucial component in drug discovery and development.Moreover, the presence of the oxadiazole moiety imparts unique electronic properties to the molecules synthesized from 3-Methyl-1,2,4-oxadiazole-5-carbaldehyde, allowing for the design of materials with specific properties, such as fluorescent probes, electron transport materials, and liquid crystals.Overall, 3-Methyl-1,2,4-oxadiazole-5-carbaldehyde plays a significant role in the field of chemical synthesis, offering chemists a valuable tool for the creation of diverse and complex organic molecules with applications across various industries.