172368-00-2

Basic information

• Product Name: 3,5-Dibromo-4-iodo-tert-butylbenzene
• Synonyms: 3,5-Dibromo-4-iodo-tert-butylbenzene
• CAS NO: 172368-00-2
• Molecular Formula: C₁₀H₁₁Br₂I
• Molecular Weight: 417.90681
• Mol File: 172368-00-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3,5-Dibromo-4-iodo-tert-butylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dibromo-4-iodo-tert-butylbenzene(172368-00-2)
• EPA Substance Registry System: 3,5-Dibromo-4-iodo-tert-butylbenzene(172368-00-2)

Safety Data

• Hazardous Substances Data: 172368-00-2(Hazardous Substances Data)

Upstream product

• 769-92-6 4-tert-Butylaniline 
• 10546-67-5 2,6-dibromo-4-(tert-butyl)aniline 

Downstream Products

• 172367-99-6 1,3-dibromo-5-tert-butyl-2-((trimethylsilyl)ethynyl)benzene 
• 1227674-33-0 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methyl radical 
• 1227674-47-6 (2,6-dibromo-4-tert-butylphenyl)(2-iodo-4-tert-butylphenyl)methyl methyl eter 
• 1227674-46-5 C₂₂H₂₆Br₂I₂O 
• 1227674-45-4 (2,6-dibromo-4-tert-butylphenyl)(2-iodo-4-tert-butylphenyl)methane 
• 1227674-44-3 C₂₁H₂₄Br₂I₂ 
• 1227674-43-2 C₂₁H₂₂Br₂I₂O 
• 1227674-41-0 C₄₂H₄₄Br₄I₂ 
• 1227674-32-9 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)diazomethane 
• 1227674-40-9 ethyl N-nitroso-N-[(2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methyl]carbamate 
• 1227674-39-6 ethyl N-[(2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methyl]carbamate 
• 1227674-38-5 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tertbutylphenyl)chloromethane 
• 1227674-37-4 (2,6-dibromo-4-tert-butylphenyl)(2,6-diiodo-4-tert-butylphenyl)methanol 
• 172368-04-6 C₄₇H₆₁N₃Si₂ 

Relevant articles and documents

Structural and electronic studies of substituted: M -terphenyl lithium complexes

The effect of para-substitution upon the structural and electronic properties of a series of m-terphenyl lithium complexes [R-Ar#-Li]2 (R = t-Bu 1, SiMe32, H 3, Cl 4, CF35; where R-Ar# = 2,6-{2,6-Xyl}2-4-R-C6H2 and 2,6-Xyl = 2,6-Me2C6H3) has been investig

Enantioposition-selective copper-catalyzed azide-alkyne cycloaddition for construction of chiral biaryl derivatives

A highly enantioposition-selective copper-catalyzed azide-alkyne cycloaddition (CuAAC) of dialkynes bearing prochiral biaryls has been developed for the construction of 1,2,3-triazoles bearing axially chiral biaryl groups in up to 76% yield and up to 99% ee.

Allosteric binding of anionic guests to a bicyclic host which imitates the action of a 'turnstile'

A bicyclic host 1, which has a diethynyl tetrafluorophenyl axis and is expected to behave as an anion-binding 'turnstile', has been designed. The Royal Society of Chemistry 2005.