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117615-77-7

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117615-77-7 Usage

Chemical structure

A pyridine derivative containing two carbonitrile groups, an ethoxy group at the 6 position, and a propyl group at the 5 position

Usage

May be used in organic synthesis and pharmaceutical research due to its unique chemical structure and properties

Potential applications

Development of new drugs, building block for the synthesis of more complex organic molecules, agrochemicals, and material science

Additional research

May reveal additional potential uses and properties of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 117615-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,7,6,1 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 117615-77:
(8*1)+(7*1)+(6*7)+(5*6)+(4*1)+(3*5)+(2*7)+(1*7)=127
127 % 10 = 7
So 117615-77-7 is a valid CAS Registry Number.

117615-77-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Ethoxy-5-propyl-3H-pyridine-2,2-dicarbonitrile

1.2 Other means of identification

Product number -
Other names -

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:117615-77-7 SDS

117615-77-7Downstream Products

117615-77-7Relevant articles and documents

1,2,3,6-Tetrahydropyridines by Cycloaddition of 1-Alkoxy-1,3-dienes and (Tosyloxyimino)malononitrile

Dormagen, Walter,Rotscheidt, Klaus,Breitmaier, Eberhard

, p. 636 - 640 (2007/10/02)

1-Alkoxy-1,3-alkadienes and 5-vinyl-3,4-dihydro-2H-pyran (prepared by Wittig carbonyl olefination of 3-alkoxyacroleins and 5-formyl-3,4-dihydro-2H-pyran) undergo cycloaddition with (tosyloxyimino)malononitrile in tetrahydrofuran/water at room temperature to give 5-alkyl-2,2-dicyano-6-ethoxy-1-tosyloxy-1,2,3,6-tetrahydropyridines and 7,7-dicyano-8-tosyloxy-3,4,6,7,8,8a-hexahydro-2H-pyranopyridine.These compounds can be converted into 6-alkoxy-5-alkyl-2,2-dicyano-2,3-dihydropyridines and pyridine-2-carboxamides, respectively.

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