22328-44-5

Basic information

• Product Name: α,α,α-<2H3>p-bromotoluene
• Synonyms: α,α,α-<2H3>p-bromotoluene
• CAS NO: 22328-44-5
• Molecular Weight: 174.013
• Mol File: 22328-44-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: α,α,α-<2H3>p-bromotoluene(CAS DataBase Reference)
• NIST Chemistry Reference: α,α,α-<2H3>p-bromotoluene(22328-44-5)
• EPA Substance Registry System: α,α,α-<2H3>p-bromotoluene(22328-44-5)

Safety Data

• Hazardous Substances Data: 22328-44-5(Hazardous Substances Data)

Upstream product

• 78585-64-5 1-bromo-4-(bromo di-deuteromethyl)benzene 
• 1124-18-1 toluene-d3 
• 865-50-9 iodomethane-d3 
• 106-37-6 1.4-dibromobenzene 
• 619-42-1 4-methoxycarbonylphenyl bromide 
• 42006-91-7 4-bromobenzyl-α,α-d₂ alcohol 

Downstream Products

• 131088-99-8 α,α,α-<2H3>p-tolunitrile 
• 78585-67-8 4-methyl-d3-benzyl alcohol 
• 114563-29-0 4-methyl-d3-benzyl bromide 
• 95249-76-6 C₁₈H₁₆⁽²⁾H₃BrO 
• 95249-74-4 C₂₁H₁₆⁽²⁾H₃BrS 
• 95249-78-8 C₁₈H₁₇⁽²⁾H₃O 
• 19315-35-6 ethyl 4-methyl-d3-benzoate 
• 95249-73-3 C₁₅H₁₂⁽²⁾H₃BrO 

Relevant articles and documents

NOVEL ORGANIC COMPOUND AND MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME AND ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME

The present invention provides a novel organic compound represented by chemical formula 1, a material for an organic electroluminescent device including the organic compound, and an organic electroluminescent device. The present invention can improve thermal stability, color purity, and device life.

Synthesis of Isotopically Labeled Tri-p-tolylamine

Three isotopically labeled tri-p-tolylamines, 15N, 15N2D2, and mono-13CH3, have been prepared using zeolite mediated bromination or nitration of toluenes as one of the key steps. The obtained 4-nitrotoluenes were reduced to 4-aminotoluenes, and coupled, v

Asymmetric Synthesis. Mechanism of Asymmetric Catalytic Allylation

The mechanism of palladium-assisted asymmetric catalytic allylation has been investigated.It is found that the process involves two primary steps: the oxidative addition of a palladium(0)-phosphine species with an allyl acetate to form diastereomeric ?-al