1250258-69-5

Basic information

• Product Name: 2-bromo-3-hexyl-5-(4-methoxyphenyl)thiophene
• Synonyms: 2-bromo-3-hexyl-5-(4-methoxyphenyl)thiophene
• CAS NO: 1250258-69-5
• Molecular Weight: 353.323
• Mol File: 1250258-69-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-bromo-3-hexyl-5-(4-methoxyphenyl)thiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-bromo-3-hexyl-5-(4-methoxyphenyl)thiophene(1250258-69-5)
• EPA Substance Registry System: 2-bromo-3-hexyl-5-(4-methoxyphenyl)thiophene(1250258-69-5)

Safety Data

• Hazardous Substances Data: 1250258-69-5(Hazardous Substances Data)

Upstream product

• 69249-61-2 3-hexyl-2-bromothiophene 
• 696-62-8 para-iodoanisole 
• 3761-92-0 n-hexylmagnesium bromide 
• 5720-07-0 4-methoxyphenylboronic acid 
• 116971-11-0 2,5-dibromo-3-hexylthiophene 
• 1693-86-3 3-hexylthiophene 

Downstream Products

• 1375353-47-1 2,3-dihexyl-5-(4-methoxyphenyl)thiophene 

Relevant articles and documents

Selective C-arylation of 2,5-dibromo-3-hexylthiophene via Suzuki cross coupling reaction and their pharmacological aspects

The present study reports the synthesis of various new derivatives based on 5-aryl-2-bromo-3-hexylthiophene with moderate-to-good yields via a palladium-catalyzed Suzuki cross-coupling reaction. This coupling method involved the reaction of 2,5-dibromo-3-

Palladium-catalyzed C-H functionalization of heteroarenes with aryl bromides and chlorides

Palladium-catalyzed C-H arylation of electron-enriched heteroarenes with aryl bromides and aryl chlorides proceeds in the presence of LiO-t-Bu as a base. The reaction allows one-pot synthesis of differently substituted 2,5-diarylthiazole with the same catalyst system by switching the solvent and the amount of base.