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33354-88-0

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33354-88-0 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.

Check Digit Verification of cas no

The CAS Registry Mumber 33354-88-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,5 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 33354-88:
(7*3)+(6*3)+(5*3)+(4*5)+(3*4)+(2*8)+(1*8)=110
110 % 10 = 0
So 33354-88-0 is a valid CAS Registry Number.

33354-88-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dipropylpyridine

1.2 Other means of identification

Product number -
Other names 2,6-di-n-propylpyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33354-88-0 SDS

33354-88-0Downstream Products

33354-88-0Relevant articles and documents

Attenuation of London Dispersion in Dichloromethane Solutions

Pollice, Robert,Bot, Marek,Kobylianskii, Ilia J.,Shenderovich, Ilya,Chen, Peter

supporting information, p. 13126 - 13140 (2017/09/26)

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.

Unprecedented double C-C bond cleavage of a cyclopentadienyl ligand

Xi, Zhenfeng,Sato, Kimihiko,Gao, Ye,Lu, Jianming,Takahashi, Tamotsu

, p. 9568 - 9569 (2007/10/03)

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

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