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Benzamide, 4-fluoro-N-[2-(1H-indol-3-yl)ethyl]-, also known as 4-Fluorobenzamide, is a chemical compound with the molecular formula C15H14FNO and a molecular weight of 239.28 g/mol. It is a white to off-white crystalline solid, soluble in organic solvents such as methanol and dimethyl sulfoxide. Benzamide, 4-fluoro-N-[2-(1H-indol-3-yl)ethyl]- is a derivative of benzamide, featuring a 4-fluorophenyl group and an indole-containing side chain. It is primarily used in the pharmaceutical industry as a research chemical and a potential drug candidate, targeting various biological pathways and receptors. Due to its unique structure, it has been studied for its potential therapeutic applications in treating various diseases, including cancer and neurological disorders. However, further research and clinical trials are needed to establish its safety and efficacy in humans.

2803-63-6

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2803-63-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2803-63-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,0 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2803-63:
(6*2)+(5*8)+(4*0)+(3*3)+(2*6)+(1*3)=76
76 % 10 = 6
So 2803-63-6 is a valid CAS Registry Number.

2803-63-6Downstream Products

2803-63-6Relevant academic research and scientific papers

An oxidative amidation and heterocyclization approach for the synthesis of β-carbolines and dihydroeudistomin y

Meruva, Suresh Babu,Raghunadh, Akula,Kamaraju, Raghavendra Rao,Kumar, U.K. Syam,Dubey

, p. 471 - 480 (2014/03/21)

A novel synthetic methodology has been developed for the synthesis of dihydro-β-carboline derivatives employing oxidative amidation-Bischler- Napieralski reaction conditions using tryptamine and 2,2-dibromo-1- phenylethanone as key starting materials. A number of dihydro-β-carboline derivatives have been synthesized in moderate to good yields using this methodology. Attempts were made towards the conversion of these dihydro-β-carbolines to naturally occurring eudistomin alkaloids.

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