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2,4-dichlorobenzaldehyde phenylhydrazone is a hydrazone derivative of 2,4-dichlorobenzaldehyde, a compound with two chlorine atoms attached to a benzene ring. It is commonly used in organic synthesis and medicinal chemistry.
Used in Organic Synthesis:
2,4-dichlorobenzaldehyde phenylhydrazone is used as a reagent for the formation of hydrazones, which are important intermediates in the synthesis of various organic compounds.
Used in Medicinal Chemistry:
2,4-dichlorobenzaldehyde phenylhydrazone is used as a visualizing agent in high-performance liquid chromatography, aiding in the detection and analysis of pharmaceutical compounds.
Used in Anti-inflammatory and Analgesic Applications:
2,4-dichlorobenzaldehyde phenylhydrazone has shown potential pharmacological activity, particularly in the area of anti-inflammatory and analgesic effects, making it a promising candidate for the development of new therapeutic agents.
Used in Research and Development:
Due to its diverse applications, 2,4-dichlorobenzaldehyde phenylhydrazone is of interest to researchers and chemists in various fields of study, including organic synthesis, medicinal chemistry, and pharmacology.

21719-63-1

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21719-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21719-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,7,1 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21719-63:
(7*2)+(6*1)+(5*7)+(4*1)+(3*9)+(2*6)+(1*3)=101
101 % 10 = 1
So 21719-63-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H10Cl2N2/c14-11-7-6-10(13(15)8-11)9-16-17-12-4-2-1-3-5-12/h1-9,17H

21719-63-1SDS

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 N-[(2,4-dichlorophenyl)methylideneamino]aniline

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:21719-63-1 SDS

21719-63-1Relevant academic research and scientific papers

Divergent construction of pyrazoles via Michael addition of n -arylhydrazones to 1,2-diaza-1,3-dienes

Mantenuto, Serena,Mantellini, Fabio,Favi, Gianfranco,Attanasi, Orazio A.

supporting information, p. 2014 - 2017 (2015/04/27)

The base (NaH)-promoted Michael addition of N-arylhydrazones (AHs) with 1,2-diaza-1,3-dienes (DDs) produces unprecedented β-azohydrazone adducts. Strategically, the use of AHs as acyl anion equivalents (d1 synthon) and DDs as α-electrophiles (a

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