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N-[2-(5-Benzyloxy-indol-3-yl)-ethyl]-benzamide is a complex organic compound with a molecular formula of C23H22N2O3. It is a derivative of benzamide, featuring a benzyloxy-indole moiety attached to the ethyl chain. N-[2-(5-benzyloxy-indol-3-yl)-ethyl]-benzamide is characterized by its potential biological activity and is often studied for its interactions with various receptors or enzymes in the field of medicinal chemistry. The presence of the benzyloxy group on the indole ring and the amide linkage to the benzene ring suggests that it may have specific pharmacological properties, making it a candidate for further investigation in drug development. The compound's structure allows for potential modifications and substitutions, which can be explored to optimize its therapeutic effects and reduce side effects.

2453-75-0

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2453-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2453-75-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,5 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2453-75:
(6*2)+(5*4)+(4*5)+(3*3)+(2*7)+(1*5)=80
80 % 10 = 0
So 2453-75-0 is a valid CAS Registry Number.

2453-75-0Downstream Products

2453-75-0Relevant academic research and scientific papers

Biocatalytic C3-Indole Methylation—A Useful Tool for the Natural-Product-Inspired Stereoselective Synthesis of Pyrroloindoles

Schneider, Pascal,Hen?en, Birgit,Paschold, Beatrix,Chapple, Benjamin P.,Schatton, Marcel,Seebeck, Florian P.,Classen, Thomas,Pietruszka, J?rg

, p. 23412 - 23418 (2021)

Enantioselective synthesis of bioactive compounds bearing a pyrroloindole framework is often laborious. In contrast, there are several S-adenosyl methionine (SAM)-dependent methyl transferases known for stereo- and regioselective methylation at the C3 position of various indoles, directly leading to the formation of the desired pyrroloindole moiety. Herein, the SAM-dependent methyl transferase PsmD from Streptomyces griseofuscus, a key enzyme in the biosynthesis of physostigmine, is characterized in detail. The biochemical properties of PsmD and its substrate scope were demonstrated. Preparative scale enzymatic methylation including SAM regeneration was achieved for three selected substrates after a design-of-experiment optimization.

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