86825-96-9

Usage

Uses

Used in Pharmaceutical Industry:
4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid is used as a building block in the synthesis of biologically active compounds, contributing to the development of new drugs. Its unique structure allows for the creation of diverse pharmaceutical agents with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid serves as a starting material for the development of new pesticides. Its chemical properties can be harnessed to design effective pest control agents, enhancing crop protection strategies.
Used in Chemical Research:
4-chlorothieno[2,3-d]pyrimidine-6-carboxylic acid is utilized in chemical research to explore its own biological activities and potential applications. Its unique structure provides a foundation for investigating new chemical reactions and syntheses, broadening the scope of chemical and pharmaceutical innovation.

Upstream product

• 14080-59-2 4-chlorothieno[2,3-d]pyrimidine 
• 124-38-9 carbon dioxide 

Downstream Products

• 871231-30-0 4-(4-fluorophenylamino)-thieno[2,3-d]pyrimidine-6-carboxylic acid 
• 1355969-46-8 (4-chlorothieno[2,3-d]pyrimidin-6-yl)(5-methoxy-1-(phenylsulfonyl)-1H-indol-2-yl)methanone 
• 1355970-33-0 benzo[b]thiophen-2-yl(4-(3-chloro-4-fluorophenylamino)thieno[2,3-d]pyrimidin-6-yl)methanone 
• 1355970-31-8 benzofuran-2-yl(4-(3-chloro-4-fluorophenylamino)thieno[2,3-d]pyrimidin-6-yl)methanone 
• 1355970-23-8 (4-((3-chloro-4-fluorophenyl)(methyl)amino)thieno[2,3-d]pyrimidin-6-yl)(1H-indol-2-yl)methanone 
• 1355970-21-6 (4-((3-chloro-4-fluorophenyl)(methyl)amino)thieno[2,3-d]pyrimidin-6-yl)(1-(phenylsulfonyl)-1H-indol-2-yl)methanone 
• 1355970-19-2 (4-(3-chloro-4-fluorophenylamino)thieno[2,3-d]pyrimidin-6-yl)(1-(phenylsulfonyl)-1H-indol-2-yl)methanone 
• 1355970-13-6 (4-(3-chloro-4-fluorophenylamino)thieno[2,3-d]pyrimidin-6-yl)(5-methoxy-1H-indol-2-yl)methanone 
• 1355970-11-4 (4-(3-chloro-4-fluorophenylamino)thieno[2,3-d]pyrimidin-6-yl)(5-hydroxy-1H-indol-2-yl)methanone 

Relevant academic research and scientific papers

Novel inhibitors of epidermal growth factor receptor: (4-(Arylamino)-7H- pyrrolo[2,3-d]pyrimidin-6-yl)(1H-indol-2-yl)methanones and (1H-indol-2-yl)(4- (phenylamino)thieno[2,3-d]pyrimidin-6-yl)methanones

Several members of the quinazoline class of known tyrosine kinase inhibitors are approved anticancer agents, often showing selectivity for receptors of the HER/ErbB-family. Combining structural elements of this class with the bisindolylmethanone-structure