265320-48-7

Basic information

• Product Name: 9-(3-bromo-4-fluorophenyl)-2,3,5,9-tetrahydro-4H-pyrano[3,4-b]thieno[2,3-e]pyridin-8(7H)-one 1,1-dioxide
• Synonyms: 9-(3-bromo-4-fluorophenyl)-2,3,5,9-tetrahydro-4H-pyrano[3,4-b]thieno[2,3-e]pyridin-8(7H)-one 1,1-dioxide
• CAS NO: 265320-48-7
• Molecular Weight: 414.252
• Mol File: 265320-48-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9-(3-bromo-4-fluorophenyl)-2,3,5,9-tetrahydro-4H-pyrano[3,4-b]thieno[2,3-e]pyridin-8(7H)-one 1,1-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(3-bromo-4-fluorophenyl)-2,3,5,9-tetrahydro-4H-pyrano[3,4-b]thieno[2,3-e]pyridin-8(7H)-one 1,1-dioxide(265320-48-7)
• EPA Substance Registry System: 9-(3-bromo-4-fluorophenyl)-2,3,5,9-tetrahydro-4H-pyrano[3,4-b]thieno[2,3-e]pyridin-8(7H)-one 1,1-dioxide(265320-48-7)

Safety Data

• Hazardous Substances Data: 265320-48-7(Hazardous Substances Data)

Upstream product

• 17115-51-4 3-oxotetrahydrothiophene dioxide 
• 77771-02-9 3-bromo-4-fluorobenzaldehyde 
• 265321-06-0 5-amino-2H-pyran-3(6H)-one 
• 688785-30-0 5-ethoxy-2H-pyran-3(6H)-one 
• 67500-49-6 methyl 2-(prop-2-yn-1-yloxy)acetate 
• 61363-56-2 2H-pyran-3,5(4H,6H)-dione 
• 61363-66-4 (2-oxopropoxy)acetic acid methyl ester 

Relevant articles and documents

Synthesis and structure-activity relationships of a novel series of tricyclic dihydropyridine-based KATP openers that potently inhibit bladder contractions in vitro

Structure-activity relationships were investigated on a novel series of tricyclic dihydropyridine-containing KATP openers. This diverse group of analogues, comprising a variety of heterocyclic rings fused to the dihydropyridine nucleus, was des

Novel radioligands and their use for identifying potassium channel modulators

The present invention relates to novel radioligands and test methods using those radioligands in screening compounds.

Pyrano, piperidino, and thiopyrano compounds and methods of use

The present invention provides novel compounds of formula I which may be useful in hyperpolarizing cell membranes, opening potassium channels, relaxing smooth muscle cells, and inhibiting bladder contractions.