122535-03-9

Basic information

• Product Name: ethyl furo[3,2-b]pyridine-6-carboxylate
• Synonyms: ethyl furo[3,2-b]pyridine-6-carboxylate;Furo[3,2-b]pyridine-6-carboxylic acid ethyl ester;Ethyl Furo[3,2-B]Pyridine-6-Carboxylate(WX618543)
• CAS NO: 122535-03-9
• Molecular Formula: C10H9NO3
• Molecular Weight: 191.18336
• EINECS: -0
• Mol File: 122535-03-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 63-65 °C(Solv: hexane (110-54-3))
• Boiling Point: 264.3±20.0 °C(Predicted)
• Appearance: /
• Density: 1.241±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 2.09±0.40(Predicted)
• CAS DataBase Reference: ethyl furo[3,2-b]pyridine-6-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl furo[3,2-b]pyridine-6-carboxylate(122535-03-9)
• EPA Substance Registry System: ethyl furo[3,2-b]pyridine-6-carboxylate(122535-03-9)

Safety Data

• Hazardous Substances Data: 122535-03-9(Hazardous Substances Data)

Usage

General Description

Ethyl furo[3,2-b]pyridine-6-carboxylate is a chemical compound with a molecular formula of C13H11NO3. It is a heterocyclic compound with a fused pyridine and furan ring system. ethyl furo[3,2-b]pyridine-6-carboxylate has been found to have potential pharmaceutical applications due to its heterocyclic structure, which is commonly found in many bioactive natural products and synthetic pharmaceuticals. Additionally, its carboxylate functional group suggests the potential for interactions with biological systems. Research on ethyl furo[3,2-b]pyridine-6-carboxylate focuses on its potential as a building block for the development of new drugs and pharmaceuticals.

Upstream product

• 80370-42-9 ethyl 2-formyl-3-oxopropanoate 
• 56267-48-2 N-(3-furyl)carbamic acid tert-butyl ester 
• 27828-71-3 5-hydroxynicotinic acid 
• 59288-38-9 ethyl 5-hydroxy-3-pyridinecarboxylate 
• 59288-40-3 ethyl 5-hydroxy-6-iodo-3-pyridinecarboxylate 

Relevant articles and documents

Synthesis method for 4-(tert-butoxycarbonyl) octahydrofuro[3,2-b] pyridine-6-carboxylic acid

The present incention relates to a synthesis method for 4-(tert-butoxycarbonyl) octahydrofuro[3,2-b] pyridine-6-carboxylic acid, and mainly solves the technical problem of no synthesis method suitable for industrialization at present. The synthesis method comprises six steps: first esterifying a compound 1 to obtain a compound 2; then performing iodination to produce a compound 3; acetylating the compound 3 to obtain a compound 4; then performing coupling to obtain a compound 5; performing cyclization to obtain a compound 6; performing hydrogenation to obtain a compound 7, then reacting with Boc anhydride to obtain a compound 8; and performing hydrogenation to obtain a final compound 9. The reaction formula is shown in the description.

Furopyridine sulfonamides and their opthalmological compositions

Furopyridine sulfonamides are carbonic anhydrase inhibitors useful in the treatment of elevated intraocular pressure and disorders associated therewith such as glaucoma.