33354-88-0

Basic information

• Product Name: 2,6-DIPROPYL PYRIDINE
• Synonyms: 2,6-DIPROPYL PYRIDINE
• CAS NO: 33354-88-0
• Molecular Formula: C₁₁H₁₇N
• Molecular Weight: 163.26
• Mol File: 33354-88-0.mol

Chemical Properties

• Boiling Point: 54-56 °C(Press: 4 Torr)
• Appearance: /
• Density: 0.900±0.06 g/cm3(Predicted)
• PKA: 6.67±0.10(Predicted)
• CAS DataBase Reference: 2,6-DIPROPYL PYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DIPROPYL PYRIDINE(33354-88-0)
• EPA Substance Registry System: 2,6-DIPROPYL PYRIDINE(33354-88-0)

Safety Data

• Hazardous Substances Data: 33354-88-0(Hazardous Substances Data)

Usage

Derived from

Pyridine

Substituents

Two propyl groups attached to the 2 and 6 positions of the pyridine ring

Uses

Perfume ingredient, flavoring agent in food products, intermediate in the synthesis of pharmaceuticals and other organic compounds

Odor

Strong, sweet, floral

Hazards

Harmful if swallowed, causes irritation if it comes into contact with the skin or eyes, proper handling and safety precautions should be taken.

Upstream product

• 2402-78-0 2,6-dichloropyridine 
• 106-94-5 propyl bromide 
• 626-05-1 2,6-Dibromopyridine 
• 156567-57-6 propylzinc bromide 
• 4663-97-2 pyridine-2,6-dicarboxylic acid diamide 
• 2893-33-6 pyridine-2,6-dinitrile 
• 109-74-0 propyl cyanide 
• 928-49-4 hex-3-yne 
• 36763-34-5 2,6-dipropionyl-pyridine 
• 108-48-5 2,6-dimethylpyridine 

Relevant articles and documents

Attenuation of London Dispersion in Dichloromethane Solutions

London dispersion constitutes one of the fundamental interaction forces between atoms and between molecules. While modern computational methods have been developed to describe the strength of dispersive interactions in the gas phase properly, the importance of inter-and intramolecular dispersion in solution remains yet to be fully understood because experimental data are still sparse in that regard. We herein report a detailed experimental and computational study of the contribution of London dispersion to the bond dissociation of proton-bound dimers, both in the gas phase and in dichloromethane solution, showing that attenuation of inter-and intramolecular dispersive interaction by solvent is large (about 70% in dichloromethane), but not complete, and that current state-of-The-Art implicit solvent models employed in quantum-mechanical computational studies treat London dispersion poorly, at least for this model system.

A switchable palladium-complexed molecular shuttle and its metastable positional isomers

We report the design, synthesis, characterization, and operation of a [2]rotaxane in which a palladium-complexed macrocycle can be translocated between 4-dimethylaminopyridine and pyridine monodentate ligand sites via reversible protonation, the metal rem

Unprecedented double C-C bond cleavage of a cyclopentadienyl ligand

Double C-C bond cleavage of a cyclopentadienyl ligand proceeded to titanacyclopentadienes when 2 equiv of nitriles were added and the resulting two-carbon unit and three-carbon unit were converted into a benzene derivative and a pyridine derivative, respectively, in one-pot. Copyright