104886-23-9

Basic information

• Product Name: Furo[3,2-b]pyridine,2,3-dihydro-3-(1-methylethyl)-(9CI)
• Synonyms: Furo[3,2-b]pyridine,2,3-dihydro-3-(1-methylethyl)-(9CI)
• CAS NO: 104886-23-9
• Molecular Formula: C10H13NO
• Molecular Weight: 163.21632
• Product Categories: ISOPROPYL
• Mol File: 104886-23-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Furo[3,2-b]pyridine,2,3-dihydro-3-(1-methylethyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Furo[3,2-b]pyridine,2,3-dihydro-3-(1-methylethyl)-(9CI)(104886-23-9)
• EPA Substance Registry System: Furo[3,2-b]pyridine,2,3-dihydro-3-(1-methylethyl)-(9CI)(104886-23-9)

Safety Data

• Hazardous Substances Data: 104886-23-9(Hazardous Substances Data)

Upstream product

• 137569-54-1 2,6-dibromo-3-pyridinyl 3-methyl-2-butenyl ether 
• 870-63-3 prenyl bromide 
• 6602-32-0 2-bromo-pyridin-3-ol 
• 6602-33-1 2,6-dibromopyridin-3-ol 
• 104886-37-5 2-bromo-3-((3-methylbut-2-en-1-yl)oxy)pyridine 

Relevant articles and documents

HETEROARYL FUSED PYRIDINES, PYRAZINES AND PYRIMIDINES AS CRF1 RECEPTOR LIGANDS

Substituted heteroaryl fused pyridine, pyrazine, and pyrimidine compounds that act as selective modulators of CRF 1 receptors are provided. These compounds are useful in the treatment of a number of CNS and periphereal disorders, particularly stress, anxi

Synthesis of a Novel Optically Active C2-Symmetric 2,2'-Bipyridine

Optically active 2,2'-bipyridine (S,S)-1 was synthesized by radical cyclization and a nickel(0)-mediated coupling of enantiomerically pure bromopyridine (S)-8.Palladium, copper, and cobalt complexes of 1 were prepared.The solid-state structures of meso-1 and 11 were determined by X-ray crystal structure analysis. Key Words: 2,2'-Bipyridine / Chiral ligand / Palladium complexes / Copper complexes / Cobalt complexes

SYNTHETIC CONNECTIONS TO THE AROMATIC DIRECTED METALATION REACTION. RADICAL-INDUCED CYCLIZATION TO SUBSTITUTED BENZOFURANS, BENZOPYRANS, AND FUROPYRIDINES

The ortho-iodoaryl allyl ethers 2, derived from 1 via the aromatic directed metalation protocol, undergo tributyl tin hydride-induced heteroring annelation to lead to unusually substituted benzofuran (3) and benzopyran, and furopyridine derivatives (Table).