1313809-70-9

Basic information

• Product Name: 6-bromo-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole
• Synonyms: 6-bromo-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole
• CAS NO: 1313809-70-9
• Molecular Weight: 370.289
• Mol File: 1313809-70-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6-bromo-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-bromo-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole(1313809-70-9)
• EPA Substance Registry System: 6-bromo-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole(1313809-70-9)

Safety Data

• Hazardous Substances Data: 1313809-70-9(Hazardous Substances Data)

Upstream product

• 21865-50-9 6-bromo-1,2,3,4-tetrahydro-9H-carbazole 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 1313809-59-4 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole 

Relevant articles and documents

Sulfoxide-TFAA and nucleophile combination as new reagent for aliphatic C-H functionalization at indole 2α-position

Aliphatic C-H functionalization at indole 2α-position mediated by acyloxythionium species 1 generated from sulfoxide and acid anhydride has been developed. The combination of sulfoxide and TFAA with O-, N- and C-nucleophiles enabled introduction of various substituents in a one-pot procedure. Especially on utilizing DMSO, the combination provided a practical and efficient method for the synthesis of a wide range of 2α-substituted indoles. The Royal Society of Chemistry 2013.