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3-((1-nitrocyclohexyl)methyl)-1H-indole is a complex organic compound characterized by a 1H-indole core, which is a bicyclic aromatic system consisting of a benzene ring fused to a pyrrole. The compound features a nitro group attached to a cyclohexane ring, which is then connected to the indole through a methylene bridge. This structure imparts unique chemical and physical properties to the molecule, making it a potential candidate for various applications in the fields of chemistry and materials science. The presence of the nitro group suggests that it may exhibit reactivity or be involved in redox processes, while the cyclohexyl ring provides a rigid, hydrophobic framework that can influence the compound's solubility and interactions with other molecules.

4771-59-9

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4771-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4771-59-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,7 and 1 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4771-59:
(6*4)+(5*7)+(4*7)+(3*1)+(2*5)+(1*9)=109
109 % 10 = 9
So 4771-59-9 is a valid CAS Registry Number.

4771-59-9Downstream Products

4771-59-9Relevant academic research and scientific papers

Catalytic and Enantioselective Control of the C–N Stereogenic Axis via the Pictet–Spengler Reaction

Kim, Ahreum,Kim, Aram,Park, Sunjung,Kim, Sangji,Jo, Hongil,Ok, Kang Min,Lee, Sang Kook,Song, Jayoung,Kwon, Yongseok

, p. 12279 - 12283 (2021)

An unprecedented example of a chiral phosphoric acid-catalyzed atroposelective Pictet–Spengler reaction of N-arylindoles is reported. Highly enantioenriched N-aryl-tetrahydro-β-carbolines with C?N bond axial chirality are obtained via dynamic kinetic reso

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