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2-(2,6-dichlorobenzylidene)hydrazinecarboxamide is a chemical compound with the molecular formula C8H6Cl2N4O. It is a derivative of hydrazinecarboxamide, featuring a 2,6-dichlorobenzene moiety attached to the molecule through a carbon-carbon double bond. 2-(2,6-dichlorobenzylidene)hydrazinecarboxamide is known for its potential applications in pharmaceuticals and agrochemicals, particularly as an intermediate in the synthesis of various biologically active compounds. Its structure provides a basis for further functionalization and modification, making it a valuable building block in the development of new drugs and pesticides. The compound's properties, such as its reactivity and stability, are influenced by the presence of the dichloro substituents, which can affect its interaction with other molecules and its overall behavior in chemical reactions.

6579-25-5

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6579-25-5 Usage

Derived from

dimethylethanolamine, parachlorophenoxyacetic acid

Type of compound

synthetic, nootropic agent

Mechanism

increases levels of neurotransmitters in the brain (e.g. acetylcholine)

Other potential effects

anti-aging, protection against oxidative stress

Available forms

tablets, capsules

Usage

dietary supplement

Check Digit Verification of cas no

The CAS Registry Mumber 6579-25-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6579-25:
(6*6)+(5*5)+(4*7)+(3*9)+(2*2)+(1*5)=125
125 % 10 = 5
So 6579-25-5 is a valid CAS Registry Number.

6579-25-5SDS

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 [(2,6-dichlorophenyl)methylideneamino]urea

1.2 Other means of identification

Product number -
Other names 2,6-Dichlorbenzaldehyd-semicarbazon

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:6579-25-5 SDS

6579-25-5Relevant academic research and scientific papers

A green approach for the synthesis of biologically active heterocyclic compounds at the platinum electrode

Sanjeev, Kumar,Srivastava

, p. 1019 - 1026 (2013/09/23)

In the present study, 2-amino-5-substituted-1,3,4-oxadiazoles (4a-k) have been synthesized by the electrochemical oxidation of semicarbazone (3a-k) using platinum anode at room temperature under controlled potential electrolysis in an undivided cell assem

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