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2719-71-3

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2719-71-3 Usage

Chemical class

Hydrazine derivative
Commonly used in organic synthesis
Contains a pyridine ring
Contains a hydrazine group
Contains a methoxybenzylidene group
Versatile compound used in medicinal chemistry and drug discovery research
Potential applications in pharmaceutical development
Studied for therapeutic properties
Valuable tool in chemical synthesis and drug development

Check Digit Verification of cas no

The CAS Registry Mumber 2719-71-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 9 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2719-71:
(6*2)+(5*7)+(4*1)+(3*9)+(2*7)+(1*1)=93
93 % 10 = 3
So 2719-71-3 is a valid CAS Registry Number.

2719-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(2-methoxyphenyl)methylideneamino]pyridin-2-amine

1.2 Other means of identification

Product number -
Other names 2-Methoxy-benzaldehyd-(N-pyrid-2-yl-hydrazon)

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:2719-71-3 SDS

2719-71-3Relevant articles and documents

Palladium-catalyzed coupling of aldehyde-derived hydrazones: Practical synthesis of triazolopyridines and related heterocycles

Thiel, Oliver R.,Achmatowicz, Michal M.,Reichelt, Andreas,Larsen, Robert D.

supporting information; experimental part, p. 8395 - 8398 (2010/12/25)

The palladium-catalyzed intermolecular coupling of aldehyde-derived hydrazones with chloroazines, followed by oxidative cyclization under mild conditions afforded access to a broad variety of bicyclic heterocyclic scaffolds (see scheme) that have potentia

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