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13472-57-6

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13472-57-6 Usage

General Description

2,6-Diethoxypyridine is a chemical compound with the molecular formula C9H13NO2. It is a basic nitrogen-containing heterocyclic compound with a pyridine ring structure. 2,6-Diethoxypyridine is primarily used as a building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its ethoxy groups make it an effective reagent in organic synthesis, and it can be used to introduce the diethoxypyridine moiety into various organic molecules. 2,6-Diethoxypyridine is a versatile and useful compound in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 13472-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,7 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13472-57:
(7*1)+(6*3)+(5*4)+(4*7)+(3*2)+(2*5)+(1*7)=96
96 % 10 = 6
So 13472-57-6 is a valid CAS Registry Number.

13472-57-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-Diethoxypyridine

1.2 Other means of identification

Product number -
Other names 2,6-DIETHOXY-PYRIDINE

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:13472-57-6 SDS

13472-57-6Relevant articles and documents

Novel synthesis method for ortho-alkane superseded pyridine

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Paragraph 0018; 0019; 0020; 0021, (2017/07/19)

The invention relates to a novel synthesis method for ortho-alkane superseded pyridine. According to the method, ortho halogenated pyridine serves as raw materials, the ortho halogenated pyridine and corresponding alcohol react to obtain the ortho-alkane superseded pyridine under the action of sodium hydroxide. The reaction has universality for the ortho halogenated pyridine, and the method is simple and practical. Influence of consumption of the sodium hydroxide on mono-substitution and di-substitution in the reaction is inspected, alkoxy mono-substitution products and alkoxy di-substitution production are acquired, and a novel simply-operated, economical and favorable process for synthesis ortho-alkane superseded pyridine is provided.

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