206559-43-5

Basic information

• Product Name: 5-BROMO-2-IODO-M-XYLENE
• Synonyms: 5-BROMO-2-IODO-1,3-XYLENE;5-BROMO-2-IODO-3-XYLENE;5-BROMO-2-IODO-M-XYLENE;5-Bromo-2-iodo-1,3-dimethylbenzene;5-Bromo-1,3-dimethyl-2-iodobenzene;2,6-diMethyl-4-broMo-iodobenzene;5-Bromo-1,3-dimethyl-2-iodobenzene 98+%;Benzene,5-broMo-2-iodo-1,3-diMethyl-
• CAS NO: 206559-43-5
• Molecular Formula: C₈H₈BrI
• Molecular Weight: 310.96
• EINECS: 1312995-182-4
• Mol File: 206559-43-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 42 °C
• Boiling Point: 282℃
• Flash Point: 125℃
• Appearance: /
• Density: 1.940
• Vapor Pressure: 0.00573mmHg at 25°C
• Refractive Index: 1.622
• Storage Temp.: Refrigerated.
• CAS DataBase Reference: 5-BROMO-2-IODO-M-XYLENE(CAS DataBase Reference)
• NIST Chemistry Reference: 5-BROMO-2-IODO-M-XYLENE(206559-43-5)
• EPA Substance Registry System: 5-BROMO-2-IODO-M-XYLENE(206559-43-5)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 206559-43-5(Hazardous Substances Data)

Usage

General Description

5-Bromo-2-iodo-m-xylene is a chemical compound with the formula C8H8BrI. It is a substituted xylene, which is a type of aromatic hydrocarbon. 5-Bromo-2-iodo-m-xylene is made up of a benzene ring with two methyl groups and two halogen atoms attached to it - one bromine and one iodine. 5-Bromo-2-iodo-m-xylene is used in various industrial applications, including as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it valuable in organic synthesis, particularly in the creation of complex molecules with specific properties. The compound has also been studied for its potential use in materials science and catalysis.

InChI:InChI=1/C8H8BrI/c1-5-3-7(9)4-6(2)8(5)10/h3-4H,1-2H3

Upstream product

• 87-62-7 2,6-dimethylaniline 
• 24596-19-8 4-bromo-2,6-dimethylphenylamine 

Downstream Products

• 404337-47-9 bis(4-bromo-2,6-dimethylphenyl)methanol 
• 404337-45-7 bis(4-bromo-2,6-dimethylphenyl)ketimine 
• 1610675-78-9 ethyl 4-bromo-2,6-dimethylphenylphosphonamide 
• 1610675-87-0 ethyl 2,6-dimethyl-4-naphthalen-2-ylphenylphosphonamide 
• 1610675-93-8 5-(phenyl)sulfanyl-7-methyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610676-03-3 7-methyl-5-phenyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610676-04-4 5-(o-methylphenyl)-7-methyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610676-05-5 5-(m-methylphenyl)-7-methyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610676-06-6 5-(p-methylphenyl)-7-methyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610676-07-7 5-(p-chlorophenyl)-7-methyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610676-08-8 5-(o,p-difluorophenyl)-7-methyl-1,2-dihydro-1-ethoxy-3H-2,1-benzazaphosphol-3-one 1-oxide 
• 1610675-73-4 ethyl 2,6-dimethyl-4-phenylsulfenylphenylphosphonamide 
• 1621681-78-4 C₁₈H₂₃O₃PS 
• 1621681-86-4 C₁₆H₁₈ClO₂PS 

Relevant articles and documents

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Spectroscopic and product studies of the effect of para substituents on the reactivity of triplet bis(2,6-dimethylphenyl)carbenes

A series of diazobis(2,6-dimethylphenyl)methanes (1) bearing eight symmetrical para di-substituents have been prepared and photolyzed to generate the corresponding carbenes (2). Product analysis studies showed that carbenes (2) decay mainly either by dimerization to form tetra(aryl)ethylene (3) or by attack at an o-methyl group to afford 1,2-dihydrobenzocyclobutenes (4) by way of o-quinodimethanes (6) in solution. The zero-field splitting parameters, D and E, were measured in matrices of different viscosities and are analyzed in terms of a sigma-dot (σ.) scale of spin-delocalization substituent constants. Fairly good correlation with σ. was found for the D values of 32 in its minimum energy geometry. Stabilities of 32 were estimated either by measuring the temperature at which the triplet carbene signals disappeared upon thawing the matrix or by analyzing the decay kinetics of 32 in a degassed solution at room temperature. They are examined in terms of the D values in matrix at low temperature and in terms of product distributions in solution at room temperature.