260355-37-1

Usage

Uses

Used in Research Applications:
1-Bromo-3,5-dimethyl-4-iodobenzene is used as a chemical intermediate for the synthesis of various organic compounds in research environments. Its reactivity allows it to participate in electrophilic substitution reactions, making it a valuable component in the development of new chemical entities.
Used in Chemical Synthesis:
In the field of organic chemistry, 1-Bromo-3,5-dimethyl-4-iodobenzene is used as a starting material for the synthesis of more complex molecules. Its presence of both bromine and iodine atoms provides opportunities for further functionalization and modification, which can be exploited in the creation of novel compounds with potential applications in various industries.
Used in Pharmaceutical Research:
1-Bromo-3,5-dimethyl-4-iodobenzene is used as a building block in the development of new pharmaceutical compounds. Its unique structure and reactivity can be harnessed to create molecules with potential therapeutic properties, contributing to the advancement of drug discovery and development.
Used in Material Science:
In the realm of material science, 1-Bromo-3,5-dimethyl-4-iodobenzene can be used to develop new materials with specific properties. Its halogenated nature may allow for the creation of materials with altered electronic, optical, or mechanical characteristics, which could be useful in various applications, such as sensors or electronic devices.

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

Upstream product

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

Downstream Products

• 943741-22-8 2-(4-bromo-2,6-dimethylphenyl)ethanol 
• 1203555-00-3 2-(4-bromo-2,6-dimethyl-phenyl)-3-methoxy-cyclopent-2-en-1-one 
• 1237529-42-8 2-(4-bromo-2,6-dimethylphenyl)cyclopent-4-ene-1,3-dione 
• 1237529-41-7 5-(4-bromo-2,6-dimethylphenyl)-4-hydroxycyclopent-2-enone 
• 1621681-76-2 C₁₂H₁₈BrO₃P 
• 1621681-86-4 C₁₆H₁₈ClO₂PS 
• 1621681-78-4 C₁₈H₂₃O₃PS 
• 1610675-73-4 ethyl 2,6-dimethyl-4-phenylsulfenylphenylphosphonamide 
• 1610676-08-8 5-(o,p-difluorophenyl)-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 
• 1610676-06-6 5-(p-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 
• 1610676-04-4 5-(o-methylphenyl)-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 

Relevant academic research and scientific papers

Asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate catalyzed by chiral Br?nsted acids

An efficient asymmetric acyl-Mannich reaction of isoquinolines with α-(diazomethyl)phosphonate and diazoacetate has been developed using chiral spiro phosphoric acids as catalysts. This reaction allowed the construction of a series of chiral 1,2-dihydroisoquinolines bearing a tertiary stereocenter at the C1 position with up to 98% yield and 99% ee.

From Naproxen Repurposing to Naproxen Analogues and Their Antiviral Activity against Influenza A Virus

The nucleoprotein (NP) of influenza A virus (IAV) required for IAV replication is a promising target for new antivirals. We previously identified by in silico screening naproxen being a dual inhibitor of NP and cyclooxygenase COX2, thus combining antivira

Π conjugated organic boron compound and its manufacturing method (by machine translation)

PROBLEM TO BE SOLVED: To synthesize a new organic boron compound that hardly has a tetra-coordination structure by subjecting a portion around boron to firm planar immobilization.SOLUTION: A specific compound is introduced into a specific boron compound,

4-PHENYLPYRANE-3,5-DIONES, 4-PHENYLTHIOPYRANE-3,5-DIONES AND 2-PHENYLCYCLOHEXANE-1,3,5-TRIONES AS HERBICIDES

Pyrandione, thiopyrandione and cyclohexanetrione compounds, which are suitable for use as herbicides.

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.