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2-(2,4-Dichlorophenyl) malondialdehyde is a chemical compound that belongs to the class of malondialdehyde derivatives. It is derived from malondialdehyde, a reactive electrophilic molecule that is involved in the formation of DNA and protein adducts. The addition of the 2,4-dichlorophenyl group to malondialdehyde increases its reactivity and toxicity, making it a compound of interest in various research applications.

74963-16-9

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74963-16-9 Usage

Uses

Used in Research Applications:
2-(2,4-Dichlorophenyl) malondialdehyde is used as a research tool for studying the effects of malondialdehyde on biological systems. Its increased reactivity compared to malondialdehyde allows for a deeper understanding of the role of malondialdehyde in various biological processes.
Used in Pathogenesis Studies:
In the field of medical research, 2-(2,4-Dichlorophenyl) malondialdehyde is used as a model compound to investigate the role of malondialdehyde in the pathogenesis of various diseases, including cancer and neurodegenerative disorders. Its enhanced reactivity aids in exploring the mechanisms by which malondialdehyde contributes to disease progression.
Used as a Biomarker for Oxidative Stress:
2-(2,4-Dichlorophenyl) malondialdehyde is being explored as a potential biomarker for oxidative stress. Its presence in biological samples can indicate the level of oxidative damage occurring within the system, providing valuable insights into the oxidative status of an organism.
Used as a Therapeutic Target for Oxidative Damage:
Due to its reactivity and involvement in oxidative processes, 2-(2,4-Dichlorophenyl) malondialdehyde is also being investigated as a therapeutic target for oxidative damage. Interventions aimed at reducing its levels or inhibiting its formation could potentially mitigate the harmful effects of oxidative stress in various conditions.
Used in Chemical Synthesis:
In the chemical industry, 2-(2,4-Dichlorophenyl) malondialdehyde may be used as an intermediate in the synthesis of other compounds, leveraging its reactivity for the creation of novel molecules with specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 74963-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,6 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74963-16:
(7*7)+(6*4)+(5*9)+(4*6)+(3*3)+(2*1)+(1*6)=159
159 % 10 = 9
So 74963-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H7ClO2/c10-9-3-1-2-7(4-9)8(5-11)6-12/h1-6,8H

74963-16-9SDS

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 2-(3-chlorophenyl)propanedial

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:74963-16-9 SDS

74963-16-9Upstream product

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