63361-61-5

Basic information

• Product Name: 3-n-butyloxypyridine
• Synonyms: 3-n-butyloxypyridine
• CAS NO: 63361-61-5
• Molecular Formula: C9H13NO
• Molecular Weight: 151
• Mol File: 63361-61-5.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 107-108 °C(Press: 13 Torr)
• Appearance: /
• Density: 0.968±0.06 g/cm3(Predicted)
• PKA: 4.77±0.10(Predicted)
• CAS DataBase Reference: 3-n-butyloxypyridine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-n-butyloxypyridine(63361-61-5)
• EPA Substance Registry System: 3-n-butyloxypyridine(63361-61-5)

Safety Data

• Hazardous Substances Data: 63361-61-5(Hazardous Substances Data)

Upstream product

• 109-00-2 3-HYDROXYPYRIDINE 
• 109-65-9 1-bromo-butane 
• 1120-90-7 3-iodopyridine 
• 71-36-3 butan-1-ol 
• 626-55-1 3-Bromopyridine 
• 626-60-8 3-Chloropyridine 

Relevant articles and documents

A Comparative Ancillary Ligand Survey in Palladium-Catalyzed C-O Cross-Coupling of Primary and Secondary Aliphatic Alcohols

The utility of RockPhos, Ad-BippyPhos, JosiPhos (CyPF-tBu), and Mor-DalPhos in palladium-catalyzed C-O cross-coupling reactions involving aliphatic alcohols and (hetero)aryl halides under analogous conditions was examined, both at room temperature and at

Alkoxylation reactions of aryl halides catalyzed by magnetic copper ferrite

Copper ferrite (CuFe2O4), which is easy-made, air-stable, low cost, easy separable, and regenerable, was applied as catalyst in an efficient method for C-O coupling reactions between various kinds of unactivated alkyl alcohols and aryl halides. This method only adopts 2.5% mol CuFe2O4 catalyst and selectively proceeds to C-O bond formation even sensitive substituents exist in the system.

A general and efficient catalyst for palladium-catalyzed C-O coupling reactions of aryl halides with primary alcohols

An efficient procedure for palladium-catalyzed coupling reactions of (hetero)aryl bromides and chlorides with primary aliphatic alcohols has been developed. Key to the success is the synthesis and exploitation of the novel bulky di-1-adamantyl-substituted bipyrazolylphosphine ligand L6. Reaction of aryl halides including activated, nonactivated, and (hetero)aryl bromides as well as aryl chlorides with primary alcohols gave the corresponding alkyl aryl ethers in high yield. Noteworthy, functionalizations of primary alcohols in the presence of secondary and tertiary alcohols proceed with excellent regioselectivity.