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1,3-bis(4-methoxyphenyl)-3-(1-methyl-1H-indol-3-yl)propan-1-one is a complex organic compound with a molecular formula of C26H25NO4. It is characterized by a propane-1-one backbone, with two 4-methoxyphenyl groups attached at the 1-position and a 1-methyl-1H-indol-3-yl group at the 3-position. 1,3-bis(4-methoxyphenyl)-3-(1-methyl-1H-indol-3-yl)propan-1-one is known for its potential applications in the field of pharmaceuticals and materials science, particularly due to its unique structure that can interact with various biological targets. The presence of methoxy groups and the indole ring system contribute to its chemical properties, making it a subject of interest for researchers exploring new drug candidates or materials with specific functionalities.

6037-61-2

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6037-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6037-61-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6037-61:
(6*6)+(5*0)+(4*3)+(3*7)+(2*6)+(1*1)=82
82 % 10 = 2
So 6037-61-2 is a valid CAS Registry Number.

6037-61-2Downstream Products

6037-61-2Relevant academic research and scientific papers

Additions of Aldehyde-Derived Radicals and Nucleophilic N-Alkylindoles to Styrenes by Photoredox Catalysis

Klussmann, Martin,Lux, Marcel

, (2020)

The consecutive addition of acyl radicals and N-alkylindole nucleophiles to styrenes was established, as well as some additional radical-nucleophile combinations. Both aryl and aliphatic aldehydes give reasonable yields. The reaction proceeds best for α-substituted styrenes, effectively creating a quaternary all-carbon center. Some iridium-based photoredox systems are catalytically active; furthermore, a base is needed in this transformation. Radicals are formed by reductive perester cleavage and hydrogen atom transfer.

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