2-(4-Methoxyphenyl)-1,3,4-oxadiazole, with the CAS number 829-35-6, is a heterocyclic organic compound characterized by the presence of an oxadiazole ring, which consists of two nitrogen atoms and three carbon atoms in a five-membered ring. This compound features a methoxy group (-OCH3) attached to a phenyl ring, which enhances its solubility and alters its electronic properties. Typically, oxadiazoles exhibit interesting biological activities, including antimicrobial and anti-inflammatory properties, making them of interest in pharmaceutical research. The presence of the methoxy group can also influence the compound's reactivity and stability. In terms of physical properties, 2-(4-methoxyphenyl)-1,3,4-oxadiazole is likely to be a solid at room temperature, with potential applications in organic electronics and as a fluorescent material due to its ability to absorb and emit light. Its synthesis often involves cyclization reactions, and it can be characterized using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity.

2-(4-methoxyphenyl)-1,3,4-oxadiazole

829-35-6: 2-(4-Methoxyphenyl)-1,3,4-oxadiazole, with the CAS number 829-35-6, is a heterocyclic organic compound characterized by the presence of an oxadiazole ring, which consists of two nitrogen atoms and three carbon atoms in a five-membered ring. This compound features a methoxy group (-OCH3) attached to a phenyl ring, which enhances its solubility and alters its electronic properties. Typically, oxadiazoles exhibit interesting biological activities, including antimicrobial and anti-inflammatory properties, making them of interest in pharmaceutical research. The presence of the methoxy group can also influence the compound's reactivity and stability. In terms of physical properties, 2-(4-methoxyphenyl)-1,3,4-oxadiazole is likely to be a solid at room temperature, with potential applications in organic electronics and as a fluorescent material due to its ability to absorb and emit light. Its synthesis often involves cyclization reactions, and it can be characterized using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity.

CAS 829-35-6

2-(4-methoxyphenyl)-1,3,4-oxadiazole

2-(4-methoxyphenyl)-1,3,4-oxadiazole

Ref: IN-DA00549J

2-(4-methoxyphenyl)-1,3,4-oxadiazole

Ref: 54-OR954531

2-(4-Methoxyphenyl)-1,3,4-oxadiazole

Ref: 10-F216489