183737-77-1

Basic information

• Product Name: 1,3-Cyclohexanedione, 2,2'-[(2-nitrophenyl)methylene]bis[5,5-dimethyl-
• CAS NO: 183737-77-1
• Molecular Formula: C23H27NO6
• Molecular Weight: 413.47
• Mol File: 183737-77-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-Cyclohexanedione, 2,2'-[(2-nitrophenyl)methylene]bis[5,5-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Cyclohexanedione, 2,2'-[(2-nitrophenyl)methylene]bis[5,5-dimethyl-(183737-77-1)
• EPA Substance Registry System: 1,3-Cyclohexanedione, 2,2'-[(2-nitrophenyl)methylene]bis[5,5-dimethyl-(183737-77-1)

Safety Data

• Hazardous Substances Data: 183737-77-1(Hazardous Substances Data)

Usage

General Description

1,3-Cyclohexanedione, 2,2'-[(2-nitrophenyl)methylene]bis[5,5-dimethyl- is a chemical compound that consists of a cyclohexanedione ring with a nitrophenyl group attached. It is commonly used as a building block in the synthesis of various organic compounds, such as pharmaceuticals and agrochemicals. 1,3-Cyclohexanedione, 2,2'-[(2-nitrophenyl)methylene]bis[5,5-dimethyl- is known for its reactivity and ability to participate in a wide range of chemical reactions, making it a valuable intermediate in the production of diverse products. Additionally, the presence of the nitrophenyl group gives the compound unique properties and potential biological activity, making it a subject of interest in medicinal chemistry and drug discovery.

Upstream product

• 126-81-8 dimedone 
• 552-89-6 2-nitro-benzaldehyde 

Downstream Products

• 162784-88-5 3,3,6,6?tetramethyl?9?(2?nitrophenyl)?3,4,6,7,9,10?hexahydroacridine?1,8(2H,5H)?dione 
• 72989-31-2 3,3-dimethyl-3,4-dihydroacridin-1(2H)-one 

Relevant articles and documents

Merging supramolecular catalysis and aminocatalysis: Amino-appended β-cyclodextrins (ACDs) as efficient and recyclable supramolecular catalysts for the synthesis of tetraketones

Well-designed amino-appended β-cyclodextrins (ACDs) with an amino side chain of different lengths at the primary face of β-CD were synthesized and employed in the catalytic synthesis of a series of tetraketones as supramolecular catalysts in water for the first time. Yields of 58-97% were obtained with up to 30 examples of substrate. The catalyst could be recycled easily, while a 92% yield and 84% rate of catalyst recovery could be achieved after 8 cycles of catalyst recycling. Moreover, a catalytic mechanism merging supramolecular catalysis and aminocatalysis could be proposed through detailed 1D and 2D NMR, ESI-MS and Job plot analyses. This protocol retained the promising characteristics of ambient temperature, green medium, simple operation, broad substrate scope, excellent yields, superb catalyst recycling performance and unique catalytic mechanism.

Application of SiO 2 nanoparticles as an efficient catalyst to develop syntheses of perimidines and tetraketones

Abstract: In this paper, we explore the catalytic activity of SiO 2 nanoparticles (NPs) as an eco-friendly, efficient and reusable catalyst in the synthesis of 2,3-dihydro-1H-perimidines as well as tetraketones. For tetraketones syntheses, a si