1402042-93-6

Basic information

• Product Name: 4-fluorobenzaldehyde 1-(5-(pyridin-3-yl)-1,3,4-thiadiazol-2-yl)hydrazone
• Synonyms: 4-fluorobenzaldehyde 1-(5-(pyridin-3-yl)-1,3,4-thiadiazol-2-yl)hydrazone
• CAS NO: 1402042-93-6
• Molecular Weight: 299.331
• Mol File: 1402042-93-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-fluorobenzaldehyde 1-(5-(pyridin-3-yl)-1,3,4-thiadiazol-2-yl)hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: 4-fluorobenzaldehyde 1-(5-(pyridin-3-yl)-1,3,4-thiadiazol-2-yl)hydrazone(1402042-93-6)
• EPA Substance Registry System: 4-fluorobenzaldehyde 1-(5-(pyridin-3-yl)-1,3,4-thiadiazol-2-yl)hydrazone(1402042-93-6)

Safety Data

• Hazardous Substances Data: 1402042-93-6(Hazardous Substances Data)

Upstream product

• 1334309-65-7 3-(5-chloro-1,3,4-thiadiazol-2-yl)pyridine 
• 299170-25-5 1-(5-(pyridine-3-yl)-1,3,4-thiadiazol-2-yl)hydrazine 
• 459-57-4 4-fluorobenzaldehyde 

Downstream Products

• 151297-75-5 3-(4-fluorophenyl)-6-(pyridine-3-yl)[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole 

Relevant articles and documents

Facile synthesis of 3,6-disubstituted-1,2,4-triazolo-[3,4-b]-1,3,4- thiadiazoles via oxidative cyclization of n-heteroaryl-substituted hydrazones and their biological activity

Fused 3,6-disubstituted triazolothiadiazoles were synthesized in good yield from a rapid and convenient oxidative cyclization of N-heteroaryl-substituted hydrazones promoted by chloramine-T trihydrate at ambient temperature. The structure of the synthesized compounds was confirmed by FTIR, 1H NMR, 13C NMR, and mass spectral data. The synthesized compounds were evaluated for their antioxidant and antitubercular activities. All the compounds 5a-i and 6a-i showed good antitubercular activity. However, only compounds 5a-i showed good antioxidant activity.