86345-44-0

Usage

Uses

Used in Medicinal Chemistry:
2-phenyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid is utilized as a key intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Drug Discovery:
In the field of drug discovery, 2-phenyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid serves as a starting point for the design and optimization of novel therapeutic agents. Its chemical properties and structural features make it a valuable candidate for the creation of new drugs with improved efficacy and selectivity.
Used in Pharmaceutical Industry:
2-phenyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid is used as a building block for the development of innovative pharmaceuticals. Its incorporation into drug molecules can lead to the discovery of new treatments for a variety of diseases and conditions.
Further research and studies are essential to fully understand the potential of 2-phenyl-4H-furo[3,2-b]pyrrole-5-carboxylic acid and to unlock its full range of applications in the medical and pharmaceutical sectors.

InChI:InChI=1/C13H9NO3/c15-13(16)10-7-12-9(14-10)6-11(17-12)8-4-2-1-3-5-8/h1-7,14H,(H,15,16)

Upstream product

• 98-80-6 phenylboronic acid 
• 1899-24-7 5-bromo-2-furancarboxaldehyde 
• 164667-60-1 methyl 2-phenyl-4H-furo[3,2-b]pyrrole-5-carboxylate 
• 71970-93-9 2-azido-3-(5-phenyl-furan-2-yl)-acrylic acid ethyl ester 
• 13803-39-9 5-phenylfuran-2-carbaldehyde 
• 71971-00-1 Ethyl 2-Phenyl-4H-furo<3,2-b>pyrrole-5-carboxylate 

Downstream Products

• 77485-00-8 2-phenyl-4H-furo<3,2-b>pyrrole 
• 106513-89-7 4-acetyl-2-phenyl-4H-furo<3,2-b>pyrrole 

Relevant academic research and scientific papers

Small molecule near-infrared boron dipyrromethene donors for organic tandem solar cells

Three furan fused boron dipyrromethenes (BODIPYs) with a CF3 group on the meso-carbon are synthesized as near-infrared absorbing materials for vacuum processable organic solar cells. The best single junction device reaches a short-circuit curre

Bright, color-tunable fluorescent dyes in the Vis/NIR region: Establishment of new "tailor-made" multicolor fluorophores based on borondipyrromethene

A new series of high-performance fluorophores named Keio Fluors (KFL), which are based on borondipyrromethene (BODIPY), are reported. The KFL dyes cover a wide spectral range from the yellow (547 nm) to the near-infrared (NIR, 738 nm) region, and their emission wavelength could be easily and subtly controlled based on simple molecular modifications only, without losing their optical properties. This "tailor-made" synthetic strategy for tuning the emission wavelength enabled the creation of fourteen KFL dyes with well-controlled emission colors (yellow, orange, red, far-red, and NIR). Moreover, these KFL dyes also retain their excellent optical properties, such as spectral bands sharper than quantum dots, high extinction coefficients (140000-316000 M-1 cm-1), and high quantum yields (0.56-0.98), without any critical solvent polarity dependent decrease of their brightness. These advantageous characteristics make the KFL dyes potentially useful as new candidates of fluorescent standard dyes to substitute or to complement existing long-wavelength fluorescent dyes, such as cyanines, oxazines, rhodamines, or other BODIPY dyes.

2-ARYLFUROPYRROLES

Preparation of ethyl 2-(4-tolyl)-4H-furopyrrole-5-carboxylate, alkylation and hydrolysis of ethyl 2-phenyl- and 2-(tolyl)furopyrrole-5-carboxylate are described.Also the synthesis of 2-phenyl- and 2-(4-tolyl)-4H-furopyrroles and their