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1-[(4-nitrobenzoyl)oxy]-2-phenyl-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37914-49-1

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37914-49-1 Usage

Appearance

Yellow solid

Solubility

Insoluble in water, soluble in organic solvents

Chemical classification

Indole derivative

Functional group

Nitrobenzoyloxy group as a substituent

Usage

Organic synthesis and pharmaceutical research

Application

Development of new drugs and pharmaceutical products

Versatility

Potential applications in various fields due to unique chemical structure and properties

Check Digit Verification of cas no

The CAS Registry Mumber 37914-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,1 and 4 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37914-49:
(7*3)+(6*7)+(5*9)+(4*1)+(3*4)+(2*4)+(1*9)=141
141 % 10 = 1
So 37914-49-1 is a valid CAS Registry Number.

37914-49-1Downstream Products

37914-49-1Relevant academic research and scientific papers

Energy Transfer Photocatalytic Radical Rearrangement in N-Indolyl Carbonates

Bera, Milan,Cho, Eun Jin,Hwang, Ho Seong,Oh, Soo Min,Shin, Seunghoon,Um, Tae-Woong

, p. 1774 - 1779 (2022/03/16)

A new type of sp3-like N-centered radical has been generated by selective energy transfer catalysis. Upon photoexcitation, homolytic N-O bond cleavage of N-indolyl carbonate in the presence of an Ir complex produced N- and O-centered radicals. The high spin density at the C3 position of indole led to radical recombination with the O-centered radical, affording valuable 3-oxyindole derivatives without decarboxylation. Transformations of the desired products into various molecules were also demonstrated.

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