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2-(2-chlorobenzylidene)-1,1-dimethylhydrazine is an organic compound with the chemical formula C9H11ClN2. It is a derivative of hydrazine, featuring a benzylidene group attached to the 2-position of the hydrazine molecule, with a chlorine atom substituting one of the hydrogen atoms on the benzene ring. 2-(2-chlorobenzylidene)-1,1-dimethylhydrazine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain pesticides. Due to its reactivity and the presence of a chlorine atom, it is important to handle 2-(2-chlorobenzylidene)-1,1-dimethylhydrazine with care, as it may pose health and environmental risks.

5051-47-8

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5051-47-8 Usage

Compound type

Hydrazine derivative

Key functional group

Chlorobenzylidene group

Backbone structure

1,1-dimethylhydrazine

Primary use

Synthesis of pharmaceutical drugs

Utility in

Medicinal and chemical applications

Potential use

Building block for synthesizing other compounds, research and development

Safety

Proper handling and precautions required

Check Digit Verification of cas no

The CAS Registry Mumber 5051-47-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,5 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5051-47:
(6*5)+(5*0)+(4*5)+(3*1)+(2*4)+(1*7)=68
68 % 10 = 8
So 5051-47-8 is a valid CAS Registry Number.

5051-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Z)-(2-chlorophenyl)methylideneamino]-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names 1-[2-(ethylpropylamino)ethyl]-1,1-dimethylhydrazinium chloride

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:5051-47-8 SDS

5051-47-8Relevant academic research and scientific papers

Synthesis of o -(dimethylamino)aryl ketones, acridones, acridinium salts, and 1 H -indazoles by the reaction of hydrazones and arynes

Dubrovskiy, Anton V.,Larock, Richard C.

, p. 11232 - 11256 (2013/02/23)

A novel, efficient route to biologically and pharmaceutically important o-(dimethylamino)aryl ketones, acridones, acridinium salts, and 1H-indazoles has been developed starting from readily available hydrazones of aldehydes and o-(trimethylsilyl)aryl triflates. The reaction proceeds through arynes under mild conditions, tolerates a wide range of functional groups, and provides the final products in good to excellent yields.

Synthesis of o -(dimethylamino)aryl ketones and acridones by the reaction of 1,1-dialkylhydrazones and arynes

Dubrovskiy, Anton V.,Larock, Richard C.

supporting information; experimental part, p. 4136 - 4139 (2011/10/12)

A novel, efficient route to biologically and pharmaceutically important o-(dimethylamino)aryl ketones and acridones has been developed starting from readily available 1,1-dimethylhydrazones of aldehydes and o-(trimethylsilyl)aryl triflates. The reaction proceeds under mild conditions, tolerates a wide range of functional groups, and provides the final products in good to excellent yields.

Synthesis of β-lactams via cycloaddition of hydrazones with phenoxyketene

Sharma,Pandhi

, p. 2196 - 2200 (2007/10/02)

Phenoxyketene is capable of annelating the disubstituted hydrazones to afford stereoselectivity cis-monocyclic β-lactams with a 1-amino functionality. The ease of cycloaddition is governed by substitutents on the azomethine carbon as well as on the hydraz

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