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(2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone is a chemical compound that features a benzene ring with an iodine atom substitution and an indole ring with a methyl group substitution. It is a member of the ketone class, characterized by a carbonyl group that is bonded to two alkyl or aryl groups. (2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone may hold promise for applications in organic synthesis, medicinal chemistry, and pharmaceutical research due to its unique structural attributes and reactivity. Further investigation into its properties is required to uncover its full potential and effects.

130259-65-3

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130259-65-3 Usage

Uses

Used in Organic Synthesis:
(2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows it to participate in a range of chemical reactions, facilitating the synthesis of complex molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone is utilized as a building block for the development of new pharmaceuticals. Its structural features may contribute to the design of molecules with specific biological activities, potentially leading to the discovery of novel therapeutic agents.
Used in Pharmaceutical Research:
(2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone is employed in pharmaceutical research as a compound of interest for its potential to be modified and optimized for various therapeutic applications. Its reactivity and structural components make it a candidate for further exploration in drug discovery processes.
Used in Chemical Research:
(2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone is also used in chemical research to study the properties and reactions of ketones, particularly those with halogen and heterocyclic substitutions. Understanding its behavior can provide insights into the broader class of ketones and their applications in chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 130259-65-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,5 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130259-65:
(8*1)+(7*3)+(6*0)+(5*2)+(4*5)+(3*9)+(2*6)+(1*5)=103
103 % 10 = 3
So 130259-65-3 is a valid CAS Registry Number.

130259-65-3Downstream Products

130259-65-3Relevant academic research and scientific papers

Aqueous intramolecular Mizoroki-Heck reaction of (2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone: A model reaction for the in situ performance evaluation of Pd catalysts

Signori, Aline M.,Latocheski, Eloah,Albuquerque, Brunno L.,Faggion, Deonildo,Bisol, Tula B.,Meier, Lidiane,Domingos, Josiel B.

, p. 1574 - 1578 (2015)

The regiospecific 5-exo intramolecular Mizoroki-Heck reaction of (2-iodophenyl)(3-methyl-1H-indol-1-yl)methanone is presented as a catalytic model reaction for the in situ performance evaluation of Pd catalysts for C-C cross-coupling reactions in aqueous medium. The reaction produces a conjugated cyclic compound which can be easily detected and quantified by UV-vis spectroscopy. Therefore, the reaction progress can be easily monitored and the catalytic parameters determined. The model reaction was tested using molecular and nanoparticulate catalysts, based on the Pd(OAc)2 salt.

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