78348-98-8

Basic information

• Product Name: Benzenemethanol, 2-bromo-a-butyl-
• CAS NO: 78348-98-8
• Molecular Formula: C11H15BrO
• Molecular Weight: 243.143
• Mol File: 78348-98-8.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 2-bromo-a-butyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 2-bromo-a-butyl-(78348-98-8)
• EPA Substance Registry System: Benzenemethanol, 2-bromo-a-butyl-(78348-98-8)

Safety Data

• Hazardous Substances Data: 78348-98-8(Hazardous Substances Data)

Upstream product

• 122-56-5 tributyl borane 
• 158918-49-1 N’-(2-bromobenzylidene)-4-methylbenzenesulfonohydrazide 
• 693-04-9 butyl magnesium bromide 
• 6630-33-7 ortho-bromobenzaldehyde 
• 78350-68-2 chlorotitanium triisopropoxide 
• 693-03-8 n-butyl magnesium bromide 
• 109-72-8 n-butyllithium 

Downstream Products

• 1338001-17-4 C₁₆H₂₃BrO₂ 
• 1338001-23-2 C₁₄H₂₃BrOSi 
• 1073174-92-1 C₁₈H₂₂O 
• 1073174-87-4 C₁₄H₂₄OSi 
• 1073174-91-0 C₁₄H₂₀O 
• 1338001-18-5 C₁₈H₃₀O₂Si 
• 73178-44-6 1-(2-methylphenyl)-1-pentanol 
• 3413-15-8 butylphthalide 
• 79784-55-7 1-(o-Cyanophenyl)-1-pentanone 
• 79784-61-5 1-(2-bromo-phenyl)-pentan-1-one 

Relevant articles and documents

SILICON-BASED CROSS COUPLING AGENTS AND METHODS OF THEIR USE

Compositions and methods using silicon-based cross-coupling agents in the formation of carbon-carbon and carbon-nitrogen bonds are described.

Cu-MEDIATED ANNULATION FOR THE EFFECTIVE SYNTHESIS OF 3-SUBSTITUTED PHTHALIDES

The present invention disclosed herein is a novel commercially feasible, one pot synthesis of library of 3-substituted phthalides of formula I via CuCN mediated oxidative cyclization in high yield. Formula I

Anion relay chemistry: Access to the type II ARC reaction manifold through a fundamentally different reaction pathway exploiting 1-oxa-2-silacyclopentanes and related congeners

Distinctly different: Two 1-oxa-2-silacyclopentenes and a saturated congener have been synthesized and demonstrated to provide access to type II anion relay chemistry (ARC) through a fundamentally new mechanistic pathway. Similar to previous studies, but contrary to initial hypothesis, Brook rearrangement additives (hexamethylphosphoramide and CuI) are necessary to promote Si migration and anion capture.