138716-23-1

Basic information

• Product Name: (E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one
• Synonyms: (E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one;(2E)-3-(DiMethylaMino)-1-(naphthalen-2-yl)prop-2-en-1-one;(2E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one;(2E)-3-(dimethylamino)-1-(2-naphthyl)prop-2-en-1-one;(E)-3-dimethylamino-1-(2-naphthyl)prop-2-en-1-one;(E)-3-dimethylamino-1-naphthalen-2-yl-prop-2-en-1-one;(E)-3-dimethylamino-1-naphthalen-2-ylprop-2-en-1-one;3-dimethylamino-1-naphthalen-2-yl-prop-2-en-1-one
• CAS NO: 138716-23-1
• Molecular Formula: C₁₅H₁₅NO
• Molecular Weight: 225
• Mol File: 138716-23-1.mol
• Article Data: 16

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one(138716-23-1)
• EPA Substance Registry System: (E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one(138716-23-1)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 138716-23-1(Hazardous Substances Data)

Usage

General Description

(E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one, also known as DMNP, is a chemical compound with the molecular formula C16H17NO. It is a yellowish powder that is insoluble in water but soluble in organic solvents. DMNP is commonly used as a fluorescent probe in biochemical and medical research, as well as in the synthesis of various organic compounds. It has also been explored for its potential applications in optical materials and as a pH indicator. Additionally, DMNP has shown promise in the development of sensors for detecting metal ions and other analytes in biological and environmental samples. Overall, (E)-3-(Dimethylamino)-1-(2-naphthyl)-2-propen-1-one has a wide range of potential applications in both scientific research and industrial processes.

Upstream product

• 613-54-7 2-Bromo-2'-acetonaphthone 
• 4637-24-5 N,N-dimethyl-formamide dimethyl acetal 
• 93-08-3 methyl 2-naphthyl ketone 

Downstream Products

• 56817-82-4 2-[(4-methylphenyl)sulfonyl]-1-(2-naphthalenyl)ethanone 
• 143620-90-0 (Z)-3-(Cyclohexyl-hydroxy-amino)-1-naphthalen-2-yl-propenone 

Relevant articles and documents

Metal-free synthesis of gem-difluorinated heterocycles from enaminones and difluorocarbene precursors

A cascade strategy to synthesise gem-difluorinated 2H-furans from reactions of BrCF2CO2Et with enaminones has been described. The reactions tolerate a wide variety of functional groups under metal-free conditions. An active aminocyclopropane is proposed to be a key intermediate through the cyclopropanation of difluorocarbene with enaminones, which further triggers a regioselective C-C bond cleavage in situ to afford the corresponding gem-difluorinated 2H-furans.

Stereoselective synthesis of trifluoromethyl-substituted 2: H -furan-amines from enaminones

A straightforward strategy for synthesis of highly functionalized trifluoromethyl 2H-furans is described. The copper catalyzed method relies on a cascade cyclic reaction between enaminones and N-tosylhydrazones. This method allows the synthesis of 2-amino

Synthesis of Polyaromatic Rings: Rh(III)-Catalyzed [5 + 1] Annulation of Enaminones with Vinyl Esters through C-H Bond Functionalization

An expedient [5 + 1] annulation method via Rh(III)-catalyzed C-H bond functionalization of enaminones to synthesize polyaromatic rings is described. The reaction tolerates a broad range of functional groups and offers a new entry to construct polycyclic a