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87894-43-7

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87894-43-7 Usage

Description

1-(2,6-dichlorobenzoyl)-3-methylindole, also known as NSC 29175, is a chemical compound characterized by a benzoyl group attached to a 3-methylindole ring, with two chlorine atoms at positions 2 and 6 of the benzoyl group. 1-(2,6-dichlorobenzoyl)-3-methylindole has garnered attention in the fields of organic synthesis and medicinal chemistry due to its potential anti-tumor, cytotoxic, anti-inflammatory, and antioxidant properties.

Uses

Used in Cancer Research:
1-(2,6-dichlorobenzoyl)-3-methylindole is used as a potential anti-tumor and cytotoxic agent for cancer research. Its application is based on its ability to exhibit anti-tumor properties, making it a subject of interest in the development of novel cancer treatments.
Used in Photodynamic Therapy:
In the medical field, 1-(2,6-dichlorobenzoyl)-3-methylindole is used as a potential photosensitizer for photodynamic therapy. The application reason is its capability to absorb light and generate reactive oxygen species, which can kill cancer cells upon light activation.
Used in Anti-inflammatory Applications:
1-(2,6-dichlorobenzoyl)-3-methylindole is used as a potential anti-inflammatory agent due to its demonstrated anti-inflammatory properties. This application is valuable in the development of new treatments for various inflammatory conditions.
Used in Antioxidant Applications:
In the pharmaceutical industry, 1-(2,6-dichlorobenzoyl)-3-methylindole is used as a potential antioxidant agent. Its application is based on its ability to neutralize harmful free radicals, which can contribute to cellular damage and various diseases.
Used in Organic Synthesis:
1-(2,6-dichlorobenzoyl)-3-methylindole is also used as a building block or intermediate in the synthesis of various organic compounds. Its application is due to its unique chemical structure, which can be further modified or functionalized to create a wide range of molecules with different properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 87894-43-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,9 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87894-43:
(7*8)+(6*7)+(5*8)+(4*9)+(3*4)+(2*4)+(1*3)=197
197 % 10 = 7
So 87894-43-7 is a valid CAS Registry Number.

87894-43-7Relevant articles and documents

Alkenylation of 1-Acylindoles with Olefins Bearing Electron-withdrawing Substituents and Palladium Acetate

Itahara, Toshio,Ikeda, Mizue,Sakakibara, Tsutomu

, p. 1361 - 1363 (2007/10/02)

The oxidation of 1-(2,6-dichlorobenzoyl)indole with olefins, such as alkyl acrylates and acrylonitrile, and palladium acetate resulted in selective 3-alkenylation of the indole nucleus.Treatment of 1-acyl-3-methylindoles under similar conditions gave the corresponding 2-alkenyl substituted indoles, while the oxidation of 6-oxo-6H-isoindoloindole gave the corresponding 3-alkenyl substituted indoles.

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