40197-02-2

Usage

Uses

Used in Pharmaceutical Industry:
3-iodo-2,5-diMethylthiophene is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure and reactivity allow for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 3-iodo-2,5-diMethylthiophene serves as a crucial building block for the synthesis of pesticides and other agrochemicals. Its properties contribute to the creation of effective and targeted pest control solutions.
Used in Materials Science:
3-iodo-2,5-diMethylthiophene is utilized as a component in the development of advanced materials, such as polymers and electronic devices. Its sulfur-containing ring imparts specific electronic properties that enhance the performance and functionality of these materials.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, 3-iodo-2,5-diMethylthiophene is employed in the creation of a wide range of chemical compounds for various applications across different industries, leveraging its unique structure and reactivity.

InChI:InChI=1/C6H7IS/c1-4-3-6(7)5(2)8-4/h3H,1-2H3

Upstream product

• 638-02-8 2,5-DIMETHYLTHIOPHENE 

Downstream Products

• 855470-64-3 2-(2,5-dimethyl-[3]thienylmercapto)-benzoic acid 
• 26421-32-9 2,5‐dimethylthiophene‐3‐carboxylic acid 
• 60813-87-8 (Z)-2-Benzylmercapto-hex-2-en-4-in 
• 96919-51-6 2,5-dimethyl-3-(o-nitrophenyl)thiophene 
• 162607-23-0 2,5-dimethylthien-3-ylboronic acid 
• 127798-29-2 3-ethynyl-2,5-dimethylthiophene 
• 1067911-54-9 3-(3,4-dimethoxyphenyl)-2,5-dimethylthiophene 
• 96919-52-7 3-(o-aminophenyl)-2,5-dimethylthiophene 
• 40197-05-5 2,5-dimethyl-3,4-diiodo-thiophene 
• 360561-24-6 1-(2,5-dimethyl-3-thienyl)-2-[2,4-dimethyl-5-(2'',4'',5''-triphenylimidazol-4'-yl)-3-thienyl]perfluorocyclopentene 

Relevant academic research and scientific papers

ROBUST PHOTOCHROMIC COMPOUNDS WITH SILICON- OR PHOSPHORUS-CONTAINING HETEROCYCLIC RING AND PRODUCTION THEREOF

In one embodiment, provided are a new class of diarylethene-containing photochromic compounds with the incorporation of silicon-or phosphorus-containing heterocycles into the "ethene" part of the diarylethene backbone that has been shown to be capable of displaying tunable, robust and thermally stable photochromic properties. Also provided are methods for synthesizing these compounds, as well as uses of these compounds as these compounds may be used as the photochromic layer in an optical recording material and other optical functioning devices.

Toward multi-addressable molecular systems: Efficient synthesis and photochromic performance of unsymmetrical bisthienylethenes

Various synthetic routes have been compared to access to unsymmetrical 1,2-bisthienylperfluorocyclopentenes having one electro-withdrawing formyl group. The strategy based on key monosusbtituted cyclopentenes appears to be the most reliable and versatile

Synthesis and photoisomerization of diarylcyclobutenes

Symmetrically and unsymmetrically substituted diarylcyclobutenes are synthesized in 20-70% yields from alkyne precursors via cobalt-catalyzed [2+2] cycloadditions. The reactions proceed under mild conditions and provide access to differently substituted diarylethene derivatives. All the diarylcyclobutene products undergo reversible photoisomerization upon irradiation with UV/Vis light. The ring-closed isomers show different thermal stabilities towards reisomerization with half-lives ranging from 9 to 300 hours. Georg Thieme Verlag Stuttgart - New York.

CHIRAL PHOSPHORATED LIGANDS USEFUL IN CATALYSTS

Described herein are new atropo-isomeric chiral phosphorated ligands having C1 symmetry, the procedure for their preparation, the organometallic complexes containing said ligands in optically active form, and the use of said complexes as catalysts in stereoselective syntheses.