84102-77-2

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 5-cyanobenzofuran-2-carboxylate is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs, contributing to the advancement of medical treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, Methyl 5-cyanobenzofuran-2-carboxylate is also used as a building block for the synthesis of various agrochemicals. Its versatile properties allow it to be incorporated into the development of new products that can enhance agricultural practices and improve crop protection.
Used in Academic Research:
Methyl 5-cyanobenzofuran-2-carboxylate may have potential applications in academic research due to its versatile properties. Researchers can explore its chemical behavior, interactions, and potential uses in various fields, contributing to the expansion of scientific knowledge and the development of innovative applications.
Used in Product Development:
Methyl 5-cyanobenzofuran-2-carboxylate's unique structure and properties also make it useful in product development. It can be incorporated into the design and synthesis of new materials and products, potentially leading to advancements in various industries and the creation of novel applications.

Upstream product

• 26028-36-4 5-bromo-2-benzofurancarboxylic acid methyl ester 
• 544-92-3 copper(I) cyanide 
• 10242-11-2 5-bromobenzo[b]furan-2-carboxylic acid 
• 1761-61-1 5-bromosalicyclaldehyde 
• 24581-99-5 methyl (4-bromo-2-formylphenoxy)acetate 

Downstream Products

• 84102-75-0 5-cyanobenzo[b]furan-2-carboxylic acid 
• 73819-60-0 5-(2-Imidazolin-2-yl)-2-<4-<4-(2-imidazolin-2-yl)phenyl>-1,3-butadienyl>-1-benzofuran 
• 84224-00-0 5-(2-Imidazolin-2-yl)-2<4-<4-(2-imidazolin-2-yl)phenyl>-(E)-vinyl>-1-benzofuran 
• 84102-80-7 <(5-Cyan-1-benzofuran-2-yl)methyl>triphenylphosphoniumchlorid 
• 84224-32-8 5-(2-Imidazolin-2-yl)-2-<4-<4-(2-imidazolin-2-yl)phenyl>-1,3-butadienyl>-1-benzofuran-dihydrochlorid 
• 84223-86-9 2-<2-(6-Amidino-1-benzofuran-2-yl)ethyl>-1-benzofuran-5-carboxamidin-dihydrochlorid 
• 84223-84-7 5-(2-Imidazolin-2-yl)-2<4-<4-(2-imidazolin-2-yl)phenyl>-(E)-vinyl>-1-benzofuran-dihydrochlorid 
• 84223-79-0 2-<2-(6-Amidino-1-benzofuran-2-yl)-(E)-vinyl>-1-benzofuran-5-carboxamidin-dihydrochlorid 
• 84224-08-8 2-<6-(4-Amidinophenyl)hexyl>-1-benzofuran-5-carboxamidin-dihydrochlorid 
• 84223-52-9 5-Amidino-1-benzofuran-2-carbaldehyd-(4-amidinophenyl)hydrazon-dihydrochlorid 
• 84224-06-6 2-<6-(4-Amidinophenyl)-1,3,5-hexatrienyl>-1-benzofuran-5-carboxamidin-dihydrochlorid 
• 84224-04-4 2-<4-(4-Amidinophenyl)butyl>-1-benzofuran-5-carboxamidin-dihydrochlorid 
• 84224-02-2 2-<4-(4-Amidinophenyl)-1,3-butadienyl>-1-benzofuran-5-carboxamidin-dihydrochlorid 
• 84224-07-7 2-<6-(4-Cyanphenyl)hexyl>-1-benzofuran-5-carbonitril 

Relevant academic research and scientific papers

Use of conformationally restricted benzamidines as arginine surrogates in the design of platelet GPIIb-IIIa receptor antagonists

The use of 5,6-bicyclic amidines as arginine surrogates in the design of a novel class of potent platelet glycoprotein IIb-IIIa receptor (GPIIb-IIIa) antagonists is described. The additional conformational restriction offered by the bicyclic nucleus results in 20-400-fold increases in potency compared to the freely flexible, acyclic benzamidine counterpart. The design, synthesis, structure-activity relationships (SAR), and in vitro activity of this novel class of GPIIb-IIIa antagonists are presented.

5,6-Bicyclic glycoprotein IIb IIIa antagonists useful in inhibition of platelet aggregation

This invention relates to 5,6 fused ring bicyclic compounds inclusive of indoles, benzofurans, and benzothiophenes, and corresponding to the formula (I) substituted with both basic (B) and acidic (A) functionality, which are useful in inhibition of platelet aggregation.

Syntheses of Biscationic, Trypanocidal 1-Benzofuran Compounds

2-Phenyl-1-benzofurans with the substituents Br, NO2, CN, and -NH2, -NH-C(=NH)-NH2, -C(=NH)-NH2, in 4',5-position were synthesized. - For arylated formamidine derivatives a simple new preparation was found by reacting amine hydrochlorides with dimethylformamide in the presence of cyanamide. - Based on 5- or 6-cyano-1-benzofuran-2-carboxylates a series of α,ω-bis(1-benzofuran-2-yl) derivatives with cyano-, amidino-, or imidazolinyl groups in 5- or 6-position was prepared.