63452-69-7

Usage

Uses

Used in Organic Synthesis:
1-IODO-4-METHOXY-2-METHYLBENZENE is used as a reagent for the introduction of the iodine group onto other molecules, which is crucial in the synthesis of various organic compounds.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1-IODO-4-METHOXY-2-METHYLBENZENE is used as a building block for the development of new drugs, given its potential biological and pharmacological properties.
Used in Research and Development:
1-IODO-4-METHOXY-2-METHYLBENZENE is also utilized in research settings to study its potential applications and effects, contributing to the advancement of knowledge in the fields of chemistry and medicine.

Upstream product

• 100-84-5 1-methoxy-3-methyl-benzene 
• 110-86-1 pyridine 
• 7553-56-2 iodine 
• 7697-37-2 nitric acid 

Downstream Products

• 938082-30-5 C₁₃H₁₈O₄ 
• 5883-96-5 5-methoxy-2-phenylindole 
• 293732-24-8 2-(bromomethyl)-1-iodo-4-methoxybenzene 
• 1527521-13-6 2-methoxy-4-methyl-7-phenyl-7H-dibenzo[c,e]azepine 
• 1374227-72-1 N'-(4-methoxy-2-methylphenyl)-N'-phenylbenzohydrazide 
• 1130283-73-6 2-iodo-5-methoxybenzamide 
• 100-84-5 1-methoxy-3-methyl-benzene 
• 141397-31-1 1-(4-methoxy-2-methylphenyl)-8-(2-methylphenyl)naphthalene 
• 54413-93-3 2-iodo-5-methoxybenzoic acid 
• 6245-57-4 4-methoxy-2-methylbenzoic acid 

Relevant academic research and scientific papers

Gold(I)-catalyzed iodination of arenes

A wide variety of electron-rich arenes were efficiently converted into the corresponding iodinated compounds via a gold(I)-catalyzed reaction under mild conditions. Georg Thieme Verlag Stuttgart. New York.

Electrophilic aromatic thallation of phenol ethers: an improved experimental procedure

In this report we present a simple modification of the classical electrophilic aromatic thallation reaction, in which iodination of several phenol ethers can be achieved in high yields under very mild reaction conditions with the mixture TTFA/BF3.Et2O/ClCH2CH2Cl, whereby both oxidative dimerizations and hydrolysis have been succesfully suppressed. - Keywords: Thallium; Electrophilic thallation; Electron-rich arenes; Aryl; Phenol

Assay for serum cholinesterase

Cholinesterase activity is determined by means of the choline obtained by the action of cholinesterase on a compound of the formula: wherein R and R1 can be the same or different, and can be alkyl, such as methyl, ethyl, propyl, butyl, isopropyl, and so forth; alkoxy, such as methoxy, ethoxy, propoxy, butoxy, and so forth; amino (-NR2R3), wherein R2 and R3 can be the same or different, and can be hydrogen, methyl, ethyl, or propyl, wherein X is an anion, such as halogen (chloro, bromo, or iodo) methyl, sulfate, nitrate and acetate;, The method of the invention ensures a conveniently low rate of cholinesterase catalyzed hydrolysis and a high degree of accuracy. Certain compounds of formula (I) defined above are novel compounds which are claimed per se.