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1,2,4,4,6-pentamethyl-1,4-dihydropyridine-3,5-dicarbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

32136-89-3

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32136-89-3 Usage

Explanation

The molecular formula represents the number of carbon (C), hydrogen (H), and nitrogen (N) atoms in the compound, which is 13, 18, and 2, respectively.

Explanation

Dihydropyridines are a class of organic compounds with a six-membered ring containing two nitrogen atoms. The compound belongs to this class.

Explanation

The core structure of the compound consists of a six-membered ring with two nitrogen atoms as part of the ring.

Explanation

The compound contains five methyl groups, which are groups of atoms consisting of three hydrogen atoms bonded to a carbon atom.

Explanation

The compound contains two cyano groups, which are functional groups consisting of a carbon atom triple-bonded to a nitrogen atom.

Explanation

Due to its unique structure and properties, the compound has potential applications in the fields of pharmaceuticals and organic synthesis.

Explanation

The compound has two types of functional groups, which are the methyl groups and the cyano groups, contributing to its chemical properties and reactivity.

Explanation

The presence of functional groups in the compound allows it to react with various reagents, making it useful in organic synthesis and pharmaceutical applications.

Explanation

The compound is relatively stable under normal conditions, which makes it suitable for use in various applications.

Explanation

The compound is likely to be soluble in organic solvents due to its nonpolar nature, which is a common characteristic of dihydropyridine derivatives.

Class

Dihydropyridine derivative

Structure

Six-membered ring with two nitrogen atoms

Methyl groups

Five

Cyano groups

Two

Potential applications

Pharmaceuticals and organic synthesis

Functional groups

Methyl and cyano groups

Chemical properties

Reactivity with various reagents

Stability

Relatively stable under normal conditions

Solubility

Soluble in organic solvents

Check Digit Verification of cas no

The CAS Registry Mumber 32136-89-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,1,3 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 32136-89:
(7*3)+(6*2)+(5*1)+(4*3)+(3*6)+(2*8)+(1*9)=93
93 % 10 = 3
So 32136-89-3 is a valid CAS Registry Number.

32136-89-3SDS

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 1,2,4,4,6-pentamethylpyridine-3,5-dicarbonitrile

1.2 Other means of identification

Product number -
Other names 1,2,4,4,6-Pentamethyl-1,4-dihydro-3,5-pyridinedicarbonitrile

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:32136-89-3 SDS

32136-89-3Downstream Products

32136-89-3Relevant academic research and scientific papers

CHEMICAL TRANSFORMATIONS OF ETHYL 3,5-DICYANO-2,4,4,6-TETRAMETHYL-1,4-DIHYDRO-1-PYRIDYL ACETATE, SYNTHESIS OF A NEW N-VINYL MONOMER

Palecek, Jaroslav,Pavlik, Manfred,Kuthan, Josef

, p. 617 - 622 (2007/10/02)

Ethoxycarbonyl group in the title compound I undergoes regioselective functional transformations to give the amide II and the carboxylic acid III.Reduction with lithium aluminium hydride gave the alcohol V whose p-toluensulfonate was converted directly or

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