114971-53-8

Usage

Uses

Used in Organic Synthesis:
2,5-DIMETHYL-4-IODOPHENOL is used as a building block in the synthesis of various organic compounds. Its unique structure allows it to serve as a versatile intermediate for the creation of a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-DIMETHYL-4-IODOPHENOL is utilized for the production of medications. Its specific chemical properties make it a valuable component in the development of new drugs with potential therapeutic benefits.
Used as a Reagent in Chemical Reactions:
2,5-DIMETHYL-4-IODOPHENOL is also employed as a reagent in various chemical reactions. Its ability to participate in different types of chemical processes makes it a useful tool for researchers and chemists in the laboratory.
Used in Research for Medicinal and Industrial Applications:
Due to its potential biological activities, 2,5-DIMETHYL-4-IODOPHENOL is a subject of research for its possible uses in medicine and industry. Its unique structure and properties hold promise for the development of new applications and products in these fields.

InChI:InChI=1/C8H9IO/c1-5-4-8(10)6(2)3-7(5)9/h3-4,10H,1-2H3

Upstream product

• 95-87-4 2,5-Dimethylphenol 

Downstream Products

• 922529-58-6 4-[1-(tert-butoxycarbonyl)-(2S)-pyrrolidinylmethoxy]-2,5-dimethyl-1-iodobenzene 
• 27023-05-8 methyl 4-hydroxy-2,5-dimethylbenzoate 
• 217660-56-5 2-(2,5-dimethyl-4-hydroxyphenyl)-6-methoxybenzo[b]thiophene 
• 1042110-06-4 5-[3-(2-{2-[2-(2-{2-[2-(2-{2-[2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)acetylamino]-ethoxy}ethoxy)ethoxy]ethoxy}ethoxy)ethoxy]ethoxy}ethoxy)propionylamino]isophthalic acid 
• 1042110-04-2 dimethyl 5-[3-(2-{2-[2-(2-{2-[2-(2-{2-[2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)acetyl-amino]ethoxy}ethoxy)ethoxy]ethoxy}ethoxy)ethoxy]ethoxy}ethoxy)propionylamino]-isophthalate 
• 1042110-63-3 4-{4-[2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)acetylamino]phenylethynyl}benzoic acid 
• 1042110-28-0 5-[2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)acetylamino]isophthalic acid 
• 1042110-59-7 2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)-N-(4-trimethylsilanylethynylphenyl)acetamide 
• 1042110-26-8 dimethyl 5-[2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)acetylamino]isophthalate 
• 1042110-61-1 N-(4-ethynylphenyl)-2-(2,5,2',4',6'-pentamethyl-biphenyl-4-yloxy)acetamide 
• 1042110-57-5 N-(4-iodophenyl)-2-(2,5,2',4',6'-pentamethylbiphenyl-4-yloxy)acetamide 
• 85223-94-5 4-hydroxy-2,5-dimethylbenzonitrile 
• 920270-43-5 1-(2-butoxyethoxy)-4-iodo-2,5-dimethylbenzene 

Relevant academic research and scientific papers

Synthesis and characterization of PPV monomer for subsequent electropolymerization

Organic synthesis of the monomer of poly(p-phenylenevinylene) was performed starting by the 2,5-dimethylphenol compound. An iodine atom was added to one end of the aromatic ring and then the iodine atom was substituted by a cyano group. Opposite to the cy

Gas-Chromatographic identifi cation of products formed in iodination of methyl phenols by retention indices

Iodination reaction followed by conversion of iodine-substituted methylphenols to the corresponding trifl uoroacetates was suggested for improving the sensitivity of the gas-chromatographic determination of phenol and its methyl-substituted derivatives (al isomers of mono- and diethylphenols, 2,3,5-, 2,3,6-, and 3,4,5-trimethylphenols) in aqueous media. Acylation products of iodo methylphenols (104 compounds) were identifi ed by linear-logarithmic retention indices on a standard nonpolar polydimethylsiloxane stationary phase, and the pattern of their variation with the number and nature of substituents were characterized. A procedure for identifi cation of methyl-substituted phenols in water in their gas-chromatographic determination with an electron-capture detector was developed. Pleiades Publishing, Ltd., 2012.

A green reagent for the iodination of phenols

A new reagent (I2/NaNO2) for the iodination of the aromatic ring of phenols has been discovered. The reaction proceeds at room temperature in 1.5-6 hours. In the presence of this reagent, iodinated compounds are regioselectively formed in significant yields from the corresponding substrates. Georg Thieme Verlag Stuttgart.

Highly selective iodination of phenols using potassium iodide and benzyltriphenylphosphonium peroxymonosulfate

An easy and selective method for monoiodination of phenols using potassium iodide in the presence of benzyltriphenylphosphonium peroxymonosulfate is presented. The reactions have been carried out in acetonitrile to afford the corresponding iodophenols in

Iodination of Phenols by Use of Benzyltrimethylammonium Dichloroiodate(1-)

The reaction of phenols with benzyltrimethylammonium dichloroiodate(1-) in dichloromethane-methanol in the presence of CaCO3 or NaHCO3 for several hours at room temperature gave iodophenols in good yields.