17452-98-1

Basic information

• Product Name: 1,3,4-Thiadiazole, 2,5-bis(4-bromophenyl)-
• CAS NO: 17452-98-1
• Molecular Formula: C14H8Br2N2S
• Molecular Weight: 396.105
• Mol File: 17452-98-1.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,3,4-Thiadiazole, 2,5-bis(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,4-Thiadiazole, 2,5-bis(4-bromophenyl)-(17452-98-1)
• EPA Substance Registry System: 1,3,4-Thiadiazole, 2,5-bis(4-bromophenyl)-(17452-98-1)

Safety Data

• Hazardous Substances Data: 17452-98-1(Hazardous Substances Data)

Upstream product

• 586-75-4 4-chlorobenzoyl chloride 
• 69673-99-0 4-bromo-N’-(4-bromobenzoyl)benzohydrazide 
• 19542-05-3 2,5-bis-(4-bromophenyl)-1,3,4-oxadiazole 
• 5933-32-4 4-bromobenzoic acid hydrazide 
• 57477-93-7 hydrazone of p-bromobenzaldehyde 
• 1122-91-4 4-bromo-benzaldehyde 

Downstream Products

• 17463-96-6 2,5-bis(4-biphenylyl)-1,3,4-thiadiazole 
• 770659-32-0 2,5-bis(4-guanylphenyl)-1,3,4-thiadiazole 
• 73819-27-9 4,4'-[1,3,4]oxadiazole-2,5-diyl-bis-benzamidine 

Relevant articles and documents

Efficient Synthesis of Conjugated 1,3,4-Thiadiazole Hybrids through Palladium-Catalyzed Cross-Coupling of 2,5-Bis(4-bromophenyl)-1,3,4-thiadiazole with Boronic Acids

New derivatives of 2,5-bis(4-heteroarylphenyl)-1,3,4-thiadiazole were synthesized under Suzuki cross-coupling reactions from 2,5-bis(4-bromophenyl)-1,3,4-thiadiazole and commercially available boronic acids. Reactions were conducted in a two-phase solvent

Synthesis of 1,3,4-thiadiazoles from aldehyde hydrazones

Reaction of p-tolualdehyde hydrazone with disulfur dichloride in the presence of DBU gave 2,5-di (p-tolyl)-1,3,4-thiadiazole (1a) in 54% yield. Phenyldiazomethane also reacted with disulfur dichloride to afford 2,5-diphenyl-1,3,4-thiadiazole (1b) in 80% y