(5-Cyclopropyl-1,2,4-oxadiazol-3-yl)methanol is a chemical compound characterized by its unique oxadiazole ring structure, which contributes to its potential biological activity. The presence of the cyclopropyl group enhances its structural complexity and may influence its reactivity and interaction with biological targets. This compound features a hydroxymethyl group, which can participate in hydrogen bonding and may enhance solubility in polar solvents. The oxadiazole moiety is known for its role in various pharmacological activities, including antimicrobial and anti-inflammatory properties. The compound's molecular structure suggests it may exhibit interesting electronic properties due to the conjugation within the oxadiazole ring. Additionally, the presence of the cyclopropyl group can impart unique steric and electronic characteristics, potentially affecting its binding affinity to biological receptors. Overall, (5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol represents a compound of interest in medicinal chemistry and drug development, warranting further investigation into its properties and applications.

(5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol

915920-06-8: (5-Cyclopropyl-1,2,4-oxadiazol-3-yl)methanol is a chemical compound characterized by its unique oxadiazole ring structure, which contributes to its potential biological activity. The presence of the cyclopropyl group enhances its structural complexity and may influence its reactivity and interaction with biological targets. This compound features a hydroxymethyl group, which can participate in hydrogen bonding and may enhance solubility in polar solvents. The oxadiazole moiety is known for its role in various pharmacological activities, including antimicrobial and anti-inflammatory properties. The compound's molecular structure suggests it may exhibit interesting electronic properties due to the conjugation within the oxadiazole ring. Additionally, the presence of the cyclopropyl group can impart unique steric and electronic characteristics, potentially affecting its binding affinity to biological receptors. Overall, (5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol represents a compound of interest in medicinal chemistry and drug development, warranting further investigation into its properties and applications.

CAS 915920-06-8

(5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol

(5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol

Ref: IN-DA00GTOU

(5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol

Ref: 10-F309471

(5-cyclopropyl-1,2,4-oxadiazol-3-yl)methanol

Ref: 3D-QLB92006