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5448-01-1

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5448-01-1 Usage

Description

(2,3-diphenyl-1H-indol-1-yl)(phenyl)methanone is a chemical compound with the molecular formula C26H20NO. It is a yellow crystalline solid that belongs to the family of indole derivatives, known for their diverse biological activities and therapeutic potential. Its structure consists of an indole ring with two phenyl groups and a phenylmethanone group attached, giving it unique pharmacological properties. (2,3-diphenyl-1H-indol-1-yl)(phenyl)methanone is used in pharmaceutical research and organic synthesis and has been studied for its potential applications in the development of drugs for various medical conditions, including cancer and depression.

Uses

Used in Pharmaceutical Research:
(2,3-diphenyl-1H-indol-1-yl)(phenyl)methanone is used as a research compound for investigating its potential applications in the development of drugs for various medical conditions. Its unique structure and pharmacological properties make it a promising candidate for further research and development.
Used in Organic Synthesis:
(2,3-diphenyl-1H-indol-1-yl)(phenyl)methanone is used as a synthetic intermediate in the preparation of other organic compounds. Its versatile structure allows for the synthesis of various derivatives with potential applications in different fields.
Used in Drug Development for Cancer:
(2,3-diphenyl-1H-indol-1-yl)(phenyl)methanone is used as a potential drug candidate for the development of cancer treatments. Its unique structure and pharmacological properties make it a promising candidate for further research and development in this area.
Used in Drug Development for Depression:
(2,3-diphenyl-1H-indol-1-yl)(phenyl)methanone is used as a potential drug candidate for the development of treatments for depression. Its unique structure and pharmacological properties make it a promising candidate for further research and development in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 5448-01-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,4 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5448-01:
(6*5)+(5*4)+(4*4)+(3*8)+(2*0)+(1*1)=91
91 % 10 = 1
So 5448-01-1 is a valid CAS Registry Number.

5448-01-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (2,3-diphenylindol-1-yl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 1-Benzoyl-2,3-diphenyl-indol

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:5448-01-1 SDS

5448-01-1Relevant articles and documents

Oxidative annulation of anilides with internal alkynes using an (Electron-Deficient η5-cyclopentadienyl)rhodium(III) catalyst under ambient conditions

Hoshino, Yuki,Shibata, Yu,Tanaka, Ken

, p. 1577 - 1585 (2014/06/09)

A dinuclear (electron-deficient η5-cyclopentadienyl) rhodium(III) complex was synthesized on a preparative scale via the rhodium-catalyzed cross [2+2+1] cyclotrimerization of silylacetylenes and two alkynyl esters, leading to substituted silylf

Indolization by Phosphorus Trichloride of Functionalized Ketone Arylhydrazones: Synthesis of Pharmacological Interesting Indoles

Baccolini, Grazieno,Dalpozzo, Renato,Todesco, Paolo E.

, p. 971 - 974 (2007/10/02)

The synthesis of indoles starting from phosphorus trichloride and arylhydrazones either functionalized in the ketone entity or N-substituted is reported.The reaction, carried out at room temperature, allows several substituents on the ketone framework of the hydrazone (e.g. ether, alkoxycarbonyl, halogeno, dialkylamino, olefinic, and phosphonic).Under optimum conditions high product yields were obtained.Evidence for the proposed mechanism is also reported.

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