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Decyl pyridine-2-carboxylate is a chemical compound with the molecular formula C15H23NO2. It is a derivative of pyridine, an aromatic heterocyclic compound, and is characterized by the presence of a carboxylate group (-COO-) attached to the pyridine ring. The decyl chain, a ten-carbon alkyl group, is attached to the pyridine ring, which contributes to the compound's lipophilic nature. This organic compound is used in various applications, including as a chemical intermediate in the synthesis of pharmaceuticals and agrochemicals, as well as in the formulation of surfactants and other specialty chemicals. Its unique structure allows it to interact with both polar and nonpolar environments, making it a versatile building block in organic synthesis.

5335-70-6

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5335-70-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5335-70-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5335-70:
(6*5)+(5*3)+(4*3)+(3*5)+(2*7)+(1*0)=86
86 % 10 = 6
So 5335-70-6 is a valid CAS Registry Number.

5335-70-6SDS

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 PICOLINIC ACID, DECYL ESTER

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylic acid,1,7,7-trimethylbicyclo[2.2.1]hept-2-yl ester

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:5335-70-6 SDS

5335-70-6Downstream Products

5335-70-6Relevant academic research and scientific papers

CeO2-catalysed one-pot selective synthesis of esters from nitriles and alcohols

Tamura, Masazumi,Tonomura, Takuya,Shimizu, Ken-Ichi,Satsuma, Atsushi

supporting information; experimental part, p. 984 - 991 (2012/06/18)

Thirteen kinds of metal oxides were tested for one-pot selective synthesis of esters from nitriles and alcohols. Ceria (CeO2) showed more than two orders of magnitude higher activity than the other oxides. CeO2 acted as a reusable and effective catalyst for the ester synthesis from various nitriles and alcohols under neutral and solvent-free conditions at 160 °C. This method provides a rare example for the synthesis of heteroaromatic esters, which have been difficult to synthesize by conventional catalytic esterification methods. Valuable esters such as picolinic acid alkyl esters and niacin benzyl esters were synthesized, demonstrating a practical aspect of the present method. Kinetic studies suggested the following reaction mechanism: (1) H2O and ROH dissociate on CeO2, (2) nucleophilic attack of hydroxyl species (OHδ-) to the adsorbed nitrile on CeO2, leading to the formation of the primary amide, (3) nucleophilic attack of alkoxide species (ORδ-) to the amide as the rate-limiting step.

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