57190-17-7

Basic information

• Product Name: 2-Bromo-1,3-diisopropylbenzene
• Synonyms: 1-Bromo-2,6-diisopropylbenzene;2,6-Diisopropylbromobenzene;2,6-Diisopropylphenyl bromide;2-Bromo-1,3-bis(1-methylethyl)benzene;2-Bromo-1,3-diisopropylbenzene;1-BroMo-2,6-diisopropylbenzene 95%;2-bromo-1,3-di(propan-2-yl)benzene
• CAS NO: 57190-17-7
• Molecular Formula: C₁₂H₁₇Br
• Molecular Weight: 241.16738
• Product Categories: Aryl;Building Blocks;C9 to C12;Chemical Synthesis;Halogenated Hydrocarbons;Organic Building Blocks
• Mol File: 57190-17-7.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 128-130℃ (15 Torr)
• Flash Point: 98°C
• Appearance: /
• Density: 1.171g/mLat 25℃
• Refractive Index: n20/D 1.532
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: 2-Bromo-1,3-diisopropylbenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-1,3-diisopropylbenzene(57190-17-7)
• EPA Substance Registry System: 2-Bromo-1,3-diisopropylbenzene(57190-17-7)

Safety Data

• Hazard Codes: Xn,N
• Statements: 22-50/53
• Safety Statements: 60-61
• RIDADR: UN 3082 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 57190-17-7(Hazardous Substances Data)

Usage

General Description

2-Bromo-1,3-diisopropylbenzene is a chemical compound with the molecular formula C12H17Br. It is a brominated aromatic compound that is commonly used in organic synthesis and as a building block for the production of various pharmaceuticals and agrochemicals. The compound is a colorless to pale yellow liquid at room temperature and has a strong aromatic odor. It is primarily used as an intermediate in the synthesis of complex organic molecules and has applications in the pharmaceutical, agrochemical, and industrial sectors. As a brominated compound, it is important to handle 2-Bromo-1,3-diisopropylbenzene with caution and under strict safety measures due to its potential health hazards and environmental impact.

Upstream product

• 24544-04-5 2,6-diisopropylbenzenamine 
• 2078-54-8 2,6-diisopropylphenol 
• 56-23-5 tetrachloromethane 
• 99-62-7 1,3-diisopropylbenzene 
• 7726-95-6 bromine 

Downstream Products

• 219838-90-1 (tetrahydrofuran-2-ylmethyl)-(2,6-diisopropylphenyl)-amine 
• 92035-95-5 2,6-bis-(1-methylethyl)benzoic acid 
• 856259-64-8 tris(2,6-diisopropylphenyl)phosphine 
• 1262046-23-0 dicyclohexyl [(2',6'-diisopropyl-3,6-dimethoxy-1-1'-biphenyl)2-yl]phosphine 
• 145967-15-3 bis(2,6-diisopropylphenyl)amine 

Relevant articles and documents

Phosphine-catalysed reductive coupling of dihalophosphanes

Classically tetraaryl diphosphanes have been synthesized through Wurtz-type reductive coupling of halophosphanes R2PX or more recently, through the dehydrocoupling of phosphines R2PH. Catalytic variants of the dehydrocoupling reactio

Linear Hydroaminoalkylation Products from Alkyl-Substituted Alkenes

The regioselective conversion of alkyl-substituted alkenes into linear hydroaminoalkylation products represents a strongly desirable synthetic transformation. In particular, such conversions of N-methylamine derivatives are of great scientific interest, because they would give direct access to important amines with unbranched alkyl chains. Herein, we present a new one-pot procedure that includes an initial alkene hydroaminoalkylation with an α-silylated amine substrate and a subsequent protodesilylation reaction that delivers linear hydroaminoalkylation products with high selectivity from simple alkyl-substituted alkenes. For that purpose, new titanium catalysts have been developed, which are able to activate the α-C?H bond of more challenging α-silylated amine substrates. In addition, a direct relationship between the ligand structure of the new catalysts and the obtained regioselectivity is described.

LUMINESCENT DIAZABENZIMIDAZOLE CARBENE METAL COMPLEXES

The present invention relates to metal-carbene complexes of the general formula (I), where variable M is Ir or Pt and that are characterized by variable R being a group of formula (a). The complexes are used in organic electronic devices, especially OLEDs (Organic Light-Emitting Diodes), illuminating elements, stationary visual display units and in material layers as emitter, charge transport material and/or charge or exiton blocker.