165534-79-2

Usage

Uses

Used in Organic Chemistry:
DIMETHYL IODOTEREPHTHALATE is used as a reagent for various synthetic reactions in organic chemistry, particularly for its ability to selectively iodinate aromatic compounds, which are crucial for the formation of iodinated products that serve as valuable intermediates for further chemical transformations.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, DIMETHYL IODOTEREPHTHALATE is utilized as an iodinating agent in the synthesis of drugs, where its selective iodination capability is essential for creating specific medicinal compounds.
Used in Agrochemical Production:
DIMETHYL IODOTEREPHTHALATE is employed in the agrochemical sector as a key component in the synthesis of various agrochemicals, contributing to the development of effective pesticides and other agricultural products.
Used in Radiopharmaceutical Preparation:
For medical imaging, DIMETHYL IODOTEREPHTHALATE is used in the preparation of radiopharmaceuticals, where its iodination properties are harnessed to label compounds for diagnostic imaging purposes.

InChI:InChI=1/C10H9IO4/c1-14-9(12)6-3-4-7(8(11)5-6)10(13)15-2/h3-5H,1-2H3

Upstream product

• 67-56-1 methanol 
• 1829-22-7 2-iodo-1,4-benzenedicarboxylic acid 
• 7647-01-0 hydrogenchloride 
• 82998-57-0 3-iodo-4-toluic acid 
• 5372-81-6 dimethyl aminoterephthalate 
• 10312-55-7 3-aminoterephthalic acid 
• 74-88-4 methyl iodide 
• 1122-42-5 2-iodo-p-xylene 

Downstream Products

• 299173-24-3 [3-iodo-4-(methoxycarbonyl)]benzoic acid 
• 583839-26-3 dimethyl 2-(phenylethynyl)terephthalate 
• 1003934-88-0 dimethyl 2-pyridin-3-ylterephthalate 
• 385416-64-8 2-iodo-1,4-benzenedicarboxaldehyde 
• 299173-16-3 methyl 4-acetyl-2-iodobenzoate 
• 299173-15-2 4-carbomethoxy-3-iodobenzoyl chloride 
• 299173-17-4 methyl 4-(1,1-difluoroethyl)-2-iodobenzoate 
• 299173-26-5 methyl 2-iodo-4-(7-hydroxy-1-oxoheptyl)benzoate 
• 299173-20-9 methyl 2-iodo-4-(7-azido-1-oxoheptyl)benzoate 
• 299173-21-0 methyl 2-iodo-4-(7-azido-1,1-difluoroheptyl)benzoate 
• 299173-19-6 methyl 2-iodo-4-(1-oxo-7-(2-tetrahydropyranyloxy)heptyl)benzoate 
• 299173-18-5 methyl 2-(3S,4R)-(3-benzyl-4-hydroxychroman-7-yl)-4-(1,1-difluoroethyl)benzoate 
• 299173-27-6 methyl 2-iodo-4-(1-oxo-7-tosyloxyheptyl)benzoate 
• 299173-22-1 methyl 2-(3S,4R)-(3-benzyl-4-hydroxychroman-7-yl)-4-(7-azido-1,1-difluoroheptyl)benzoate 

Relevant academic research and scientific papers

Synthesis and Dynamics of Nanosized Phenylene-Ethynylene-Butadiynylene Rotaxanes and the Role of Shape Persistence

Phenylacetylene-based [2]rotaxanes were synthesized by a covalent-template approach by aminolysis of the corresponding prerotaxanes. The wheel and the bulky stoppers are made of phenylene-ethynylene-butadiynylene macrocycles of the same size. The stoppers

Synthesis and evaluation of N-alkyl-9-aminoacridines with antibacterial activity

A series of 9-alkylaminoacridines were synthesized and evaluated for activity against two strains of methicillin-resistant and one strain of methicillin-sensitive Staphylococcus aureus. Results are presented that show a clear structure activity relationship between the N-alkyl chain length and antibacterial activity with peak MIC99 values of 2-3 μM for alkyl chains ranging from 10 to 14 carbons in length. Although prior work has linked the function of acridine-based compounds to intercalation and topoisomerase inhibition, the present results show that 9-alkylaminoacridines likely function as amphiphilic membrane-active disruptors potentially in a similar manner as quaternary ammonium antimicrobials.

Synthesis and flame retardant testing of new boronated and phosphonated aromatic compounds

The present report describes the preparation and use of some dimethyl terephthalate derivatives in transition metal-catalyzed coupling reactions to produce new reactive flame retardants. Dimethyl iodoterephthalate and dimethyl 2,5-diiodoterephthalate were

Chiral donor photoinduced-electron-transfer (d-PET) boronic acid chemosensors for the selective recognition of tartaric acids, disaccharides, and ginsenosides

A modular approach was proposed for the preparation of chiral fluorescent molecular sensors, in which the fluorophore, scaffold, and chirogenic center can be connected by ethynyl groups, and these modules can easily be changed to other structures to optim