19259-05-3

Usage

Structure

A five-membered heterocyclic ring consisting of four carbon atoms and one sulfur atom, with two iodine atoms attached to adjacent carbon atoms.

Properties

2,3-Diiodothiophene exhibits excellent electron-donating properties, making it useful in the development of organic electronics and optoelectronic devices.

Applications

Commonly used as a building block for the synthesis of various organic compounds and materials.

Interest

Its unique chemical structure and reactivity have attracted interest in the fields of pharmaceuticals and fine chemicals.

Hazards

2,3-Diiodothiophene is a hazardous chemical and should be handled with caution due to its toxic and potentially harmful effects on human health and the environment.

Upstream product

• 188290-36-0 thiophene 
• 927-84-4 bis(trifluoromethyl)peroxide 
• 872-31-1 3-Bromothiophene 

Downstream Products

• 60166-84-9 3-iodo-thiophene-2-carboxylic acid 
• 1030610-28-6 C₄₂H₅₂SSi₂ 
• 1182318-31-5 4,11-diphenyl-6,7,8,9-tetrapropyl-5,10-dihydroanthra[2,3-b]thiophene 
• 1182318-33-7 4,11-diphenyl-5,10-dihydroanthra[2,3-b]thiophene 

Relevant academic research and scientific papers

Co-thermolysis: A one-pot synthetic method for novel 2-substituted-5- (trifluoromethoxy)thiophenes

A new 'green' process to obtain trifluoromethoxylated compounds by a gas-phase method has been accomplished. Through it, new 2-substituted-5- (trifluoromethoxy)thiophenes have been obtained in moderate to good yields. Though the reaction occurs in the gas-phase and radicals are involved, an electron transfer mechanism is also postulated to explain the appearance of all detected products.

Selective metallation of 3-halothiophenes: Practical methods for the synthesis of 2-bromo-3-formylthiophene

Selective lithiation of 3-bromothiophene was accomplished under controlled conditions without formation of undesired thienyllithium compounds. A thienyl Grignard reagent derived from 2-bromo-3-iodothiophene was transformed into 2-bromo-3-formylthiophene in high selectivity by formylation with dimethylformamide (DMF) at optimal reaction temperature. Copyright Taylor & Francis Group, LLC.