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56394-24-2

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56394-24-2 Usage

Description

6-Chloro-3-cyano-4-methylcoumarin is an organic compound with the chemical formula C11H6ClNO2. It is a derivative of coumarin, a natural compound found in many plants. This chemical is known for its fluorescent properties and potential applications in biomedical research and pharmaceutical development.

Uses

Used in Biomedical Research:
6-Chloro-3-cyano-4-methylcoumarin is used as a fluorescent probe for detecting and measuring the presence of various reactive oxygen and nitrogen species in biological systems. Its ability to fluoresce upon interaction with these species makes it a valuable tool for studying oxidative stress and related biological processes.
Used in Pharmaceutical Development:
6-Chloro-3-cyano-4-methylcoumarin has been studied for its potential use as a fluorescent indicator for the detection of zinc ions. Zinc is an essential trace element involved in numerous biological functions, and its detection is important for understanding its role in health and disease.
Used in Antimicrobial Applications:
6-Chloro-3-cyano-4-methylcoumarin has been investigated for its antimicrobial activities, showing promising results in inhibiting the growth of certain bacteria. This property could be useful in the development of new antibiotics or disinfectants to combat bacterial infections.
Used in Anticancer Applications:
6-Chloro-3-cyano-4-methylcoumarin has also been studied for its potential anticancer activities, with research indicating that it can inhibit the growth of certain cancer cells. Further investigation into its mechanism of action and potential therapeutic applications could lead to the development of new cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 56394-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,3,9 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56394-24:
(7*5)+(6*6)+(5*3)+(4*9)+(3*4)+(2*2)+(1*4)=142
142 % 10 = 2
So 56394-24-2 is a valid CAS Registry Number.

56394-24-2SDS

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 6-chloro-4-methyl-2-oxochromene-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 6-CHLORO-4-METHYL-2-OXO-2H-CHROMENE-3-CARBONITRILE

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:56394-24-2 SDS

56394-24-2Relevant articles and documents

Palladium-Catalyzed Regioselective and Diastereoselective C-Glycosylation by Allyl-Allyl Coupling

Li, Junhao,Zheng, Nan,Duan, Xuelun,Li, Rui,Song, Wangze

supporting information, p. 846 - 850 (2020/12/13)

A Pd-catalyzed C-glycosylation reaction was developed by allyl-allyl coupling process using Achmatowicz rearrangement products as donors and methylcoumarins as acceptors under mild conditions. This method featured regio- and diastereoselectivities, stereo

Synthesis and biological evaluation of 4-styrylcoumarin derivatives as inhibitors of TNF-α and IL-6 with anti-tubercular activity

Upadhyay, Kuldip,Bavishi, Abhay,Thakrar, Shailesh,Radadiya, Ashish,Vala, Hardevsinh,Parekh, Shrey,Bhavsar, Dhairya,Savant, Mahesh,Parmar, Manisha,Adlakha, Priti,Shah, Anamik

supporting information; experimental part, p. 2547 - 2549 (2011/05/15)

A series of 4-styrylcoumarin have been synthesized by Knoevenagel condensation between substituted 4-methylcoumarin-3-carbonitrile and different heterocyclic or aromatic aldehydes. 4-Methylcoumarin-3-carbonitrile has been synthesized by the base catalyzed reaction between substituted 2-hydroxyacetophenone and ethyl cyanoacetate. The structures of the newly synthesized compounds were confirmed by 1H NMR, IR and mass spectral analysis. All the compounds were evaluated for their anti-inflammatory activity (against TNF-α and IL-6) and anti-tubercular activity. Compounds 6a, 6h and 6j exhibited promising activity against IL-6 with 72-87% inhibition and compound 6v showed potent activity against TNF-α with 73% inhibition at 10 μM concentration. Whereas compounds 6n, 6o, 6r and 6u showed very good anti-tubercular activity against Mycobacterium tuberculosis H37Rv strain at 6.25 μM.

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