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5,6-dimethoxy-2-phenyl-1H-indene-1,3(2H)-dione is a complex organic compound with the molecular formula C17H14O4. It is characterized by a 1H-indene core structure, which is a type of aromatic hydrocarbon with a cyclohexene ring fused to a benzene ring. The compound features two methoxy groups (-OCH3) at the 5 and 6 positions, which are electron-donating groups that can influence the compound's reactivity and solubility. Additionally, a phenyl group (C6H5) is attached at the 2 position, contributing to the compound's aromaticity and potentially affecting its physical properties. The 1,3-dione functional group, which consists of two carbonyl groups (C=O) separated by a single carbon atom, is present in the molecule, endowing it with specific chemical reactivity. 5,6-dimethoxy-2-phenyl-1H-indene-1,3(2H)-dione is likely to be used in the synthesis of various pharmaceuticals, dyes, or other organic compounds due to its unique structure and functional groups.

4087-85-8

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4087-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4087-85-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,8 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4087-85:
(6*4)+(5*0)+(4*8)+(3*7)+(2*8)+(1*5)=98
98 % 10 = 8
So 4087-85-8 is a valid CAS Registry Number.

4087-85-8Downstream Products

4087-85-8Relevant academic research and scientific papers

Synthesis of Core-Modified Third-Generation Light-Driven Molecular Motors

Berrocal, José Augusto,Pfeifer, Lukas,Heijnen, Dorus,Feringa, Ben L.

, p. 10670 - 10680 (2020)

The synthesis and characterization of a series of light-driven third-generation molecular motors featuring various structural modifications at the central aromatic core are presented. We explore a number of substitution patterns, such as 1,2-dimethoxybenzene, naphthyl, 1,2-dichlorobenzene, 1,1′:2′,1″-terphenyl, 4,4″-dimethoxy-1,1':2′,1″-terphenyl, and 1,2-dicarbomethoxybenzene, considered essential for designing future responsive systems. In many cases, the synthetic routes for both synthetic intermediates and motors reported here are modular, allowing for their post-functionalization. The structural modifications introduced in the core of the motors result in improved solubility and a bathochromic shift of the absorption maxima. These features, in combination with a structural design that presents remote functionalization of the stator with respect to the fluorene rotors, make these novel motors particularly promising as light-responsive actuators in covalent and supramolecular materials.

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