37052-98-5

Basic information

• Product Name: 2-phenylfuro[2,3-b]quinoxaline
• CAS NO: 37052-98-5
• Molecular Formula: C₁₆H₁₀N₂O
• Molecular Weight: 246.2634
• Mol File: 37052-98-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 443.2°C at 760 mmHg
• Flash Point: 226.1°C
• Density: 1.281g/cm³
• Vapor Pressure: 1.23E-07mmHg at 25°C
• Refractive Index: 1.708
• CAS DataBase Reference: 2-phenylfuro[2,3-b]quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-phenylfuro[2,3-b]quinoxaline(37052-98-5)
• EPA Substance Registry System: 2-phenylfuro[2,3-b]quinoxaline(37052-98-5)

Safety Data

• Hazardous Substances Data: 37052-98-5(Hazardous Substances Data)

Upstream product

• 132467-02-8 3-(β-chloro-styryl)-1H-quinoxalin-2-one 
• 83451-41-6 3-(α,β-dibromo-phenethyl)-1H-quinoxalin-2-one 
• 98-95-3 nitrobenzene 
• 121-44-8 triethylamine 
• 2213-63-0 2,3-dichloroquinoxaline 
• 536-74-3 phenylacetylene 
• 924-44-7 glyoxylic acid ethyl ester 
• 95-54-5 1,2-diamino-benzene 
• 861310-73-8 3,4-dibromo-2-oxo-4-phenyl-butyric acid 
• 101423-50-1 3-(α,β-dichloro-phenethyl)-1H-quinoxalin-2-one 
• 75303-08-1 (E)-3-styrylquinoxalin-2(1H)-one 
• 5817-92-5 2,4-dioxo-4-phenylbutanoic acid 
• 1448-87-9 2-chloroquinoxaline 
• 98-86-2 acetophenone 

Downstream Products

• 135226-50-5 4,9-Diacetyl-4,9-dihydro-2-phenylfuro<2,3-b>quinoxaline 
• 88051-11-0 3-bromo-2-phenylfuro<2,3-b>quinoxaline 

Relevant articles and documents

Synthesis and photophysical properties of selenopheno[2,3-b]quinoxaline and selenopheno[2,3-b]pyrazine heteroacenes

In this paper, we report the novel synthesis of three different heterocycles, namely 2-arylselenopheno[2,3-b]quinoxaline, 3-(aryl/alkylselanyl)-2-arylselenopheno[2,3-b]quinoxaline and 6-phenyl-7-(arylselanyl)selenopheno[2,3-b]pyrazine derivatives, from th

Trifluoroacetic Acid Mediated One-Pot Synthesis of Furo-Fused Quinoxalines/Pyrazines

A trifluoroacetic acid promoted step-economical one-pot approach to the synthesis of furo-fused quinoxalines/pyrazines by the reaction of 2,3-dichloroquinoxalines/pyrazines with alkynes is described. The reaction involves a selective in-situ Sonogashira c

Transition metal free hydrolysis/cyclization strategy in a single pot: Synthesis of fused furo N-heterocycles of pharmacological interest

A transition metal free tandem two-step strategy has been developed involving hydrolysis of 2-chloro-3-alkynyl quinoxalines/pyrazines followed by in situ cyclization of the corresponding 2-hydroxy-3-alkynyl intermediates in a single pot leading to fused furo N-heterocycles as potential inhibitors of sirtuins. A representative compound showed promising pharmacological properties in vitro and in vivo.