699119-05-6

Basic information

• Product Name: 1-BROMO-2,5-DIMETHYL-4-IODOBENZENE
• Synonyms: 1-BROMO-2,5-DIMETHYL-4-IODOBENZENE;1-broMo-4-iodo-2,5-diMethylbenzene
• CAS NO: 699119-05-6
• Molecular Formula: C₈H₈BrI
• Molecular Weight: 310.96
• Product Categories: Bromine Compounds;Iodine Compounds
• Mol File: 699119-05-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-BROMO-2,5-DIMETHYL-4-IODOBENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-BROMO-2,5-DIMETHYL-4-IODOBENZENE(699119-05-6)
• EPA Substance Registry System: 1-BROMO-2,5-DIMETHYL-4-IODOBENZENE(699119-05-6)

Safety Data

• Hazardous Substances Data: 699119-05-6(Hazardous Substances Data)

Usage

General Description

1-Bromo-2,5-dimethyl-4-iodobenzene, also known as 4-bromo-2,5-dimethyliodobenzene, is a chemical compound with the molecular formula C8H9BrI. It is a derivative of benzene and belongs to the class of haloarenes. This chemical is commonly used as an intermediate in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fine chemicals. It is a white to light yellow solid at room temperature and is soluble in common organic solvents. 1-Bromo-2,5-dimethyl-4-iodobenzene is primarily used as a reagent in chemical reactions, such as cross-coupling reactions and nucleophilic aromatic substitution. It is important to handle this compound with care, as it is considered to be potentially hazardous to health and the environment.

Upstream product

• 1122-42-5 2-iodo-p-xylene 
• 553-94-6 4-bromo-m-xylene 
• 1074-24-4 2,5-dibromo-p-xylene 
• 589-87-7 1,4-bromoiodobenzene 
• 37614-58-7 3-(4-bromophenyl)prop-2-yn-1-ol 
• 1228259-49-1 9,9,10,10,11,11,12,12,13,13,14,14,14-tridecafluoro-6-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctyl)tetradec-1-yne 
• 114091-36-0 tributyl(trimethylgermyl)stannane 

Downstream Products

• 1426563-42-9 ((4-bromo-2,5-dimethylphenyl)ethynyl)triisopropylsilane 
• 931120-78-4 3-(4-bromo-2,5-dimethyl-phenyl)-5-isopropenyl-2-methyl-cyclohex-2-enone 
• 931120-70-6 1-(4-bromo-2,5-dimethyl-phenyl)-5-isopropenyl-2-methyl-cyclohex-2-enol 

Relevant articles and documents

Pushing the synthetic limit: Polyphenylene dendrimers with "exploded" branching units - 22-nm-diameter, monodisperse, stiff macromolecules

(Figure Presented) Structural perfection up to the fifth generation of a polyphenylene dendrimer has been achieved by inserting p-terphenyl spacers into the arms of each branching unit (see picture). The stiff, monodisperse macromolecules with diameters u

Synthesis and properties of metal-ligand complexes with endohedral amine functionality

A series of tetracationic M2L4 palladium-pyridyl complexes with endohedral amine functionality have been synthesized. The complexes were analyzed by NMR techniques (including Diffusion NMR and 2D NOESY), electrospray ionization (ESI) mass spectrometry, and X-ray crystallography. The solid state analysis shows a large change in crystal morphology upon introduction of the endohedral amine groups, caused by deleterious interactions between the amines and the triflate counterions from the coordination process. Combination of different ligands allows analysis of ligand exchange rates via NMR analysis, with half-lives on the order of 3 h, independent of the donor properties of the ligand. Self-sorting behavior is observed, with more electron-rich ligands being favored. The amine-containing and extended complexes are strongly fluorescent, giving quantum yields of up to 83%.