76469-33-5

Basic information

• Product Name: Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI)
• Synonyms: Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI);2-Chloro-1-naphthalen-1-yl-ethanone;2-chloro-1-(naphthalen-1-yl)ethan-1-one
• CAS NO: 76469-33-5
• Molecular Formula: C₁₂H₉ClO
• Molecular Weight: 204.65226
• Product Categories: ACETYLHALIDE
• Mol File: 76469-33-5.mol
• Article Data: 8

Chemical Properties

• Melting Point: 40-41.5 °C
• Boiling Point: 204-205 °C(Press: 18 Torr)
• Appearance: /
• Density: 1.229±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI)(76469-33-5)
• EPA Substance Registry System: Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI)(76469-33-5)

Safety Data

• Hazardous Substances Data: 76469-33-5(Hazardous Substances Data)

Usage

General Description

Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI) is a chemical compound with the molecular formula C16H11ClO. It consists of a chloro-substituted naphthalene ring attached to a ketone functional group. Ethanone, 2-chloro-1-(1-naphthalenyl)- (9CI) is commonly used in the synthesis of various organic materials and pharmaceuticals. It has also been studied for its potential biological and pharmacological activities. However, there is limited information available about its specific properties and uses, making it a less well-known chemical compound in the scientific community. Further research and investigation are needed to fully understand its potential applications and effects.

Upstream product

• 826-74-4 1-vinylnaphthalene 
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• 60-29-7 diethyl ether 

Downstream Products

• 86-55-5 1-naphthalenecarboxylic acid 
• 80749-33-3 (2-methyl-1H-indol-3-yl)(naphthalen-1-yl) methanone 
• 1215004-64-0 (naphthalen-1-yl)(2-phenyl-1H-indol-3-yl)methanone 
• 941-98-0 1'-naphthacetophenone 
• 57605-95-5 1-(1-naphthyl)ethanol 
• 4653-13-8 4-(1-naphthyl)-4-oxobutanoic acid 
• 861330-63-4 (2-[1]naphthyl-2-oxo-ethyl)-malonic acid 

Relevant articles and documents

OLED electron transport material as well as preparation method and application thereof (by machine translation)

The invention belongs to the technical field of organic electronic transmission materials, and relates to OLED electron transport materials as well as a preparation method and application thereof. OLED (Organic Light Emitting Diode) electron transport material in particular relates to a small molecule OLED material with an asymmetric structure containing a benzoxazole group on one side and an aryl group with electron transport performance at one side. As the electron transport material is applied to OLED devices, good device performance and lower driving voltage can be obtained; meanwhile, the luminous efficiency and the service life of the device are greatly improved. (by machine translation)

Asymmetric transfer hydrogenation of 1-naphthyl ketones by an ansa-Ru(II) complex of a DPEN-SO2N(Me)-(CH2)2(η 6-p-tol) combined ligand

The first second-generation designer Ru(II) catalyst 1b featuring an enantiopure N,C-(N-ethylene-N-methyl-sulfamoyl)-tethered (DPEN- κ2N,N′)/η6-toluene hybrid ligand is introduced. Using an S/C = 1000 in HCO2H-Et3N 5:2 transfer hydrogenation medium, secondary 1-naphthyl alcohols are obtained in up to >99.9% ee under mild conditions. Mechanistic factors are discussed.

Synthetic Studies on Indoles and Related Compounds. XV. An Unusual Acylation of Ethyl Indole-2-Carboxylate in the Friedel-Crafts Acylation

The Friedel-Crafts reaction of ethyl indole-2-carboxylate (1a) with acyl chlorides or acid anhydrides in the presence of Lewis acids was investigated in order to establish a preparative procedure for the corresponding ethyl 3-acylindole-2-carboxylates (4).Although monoacylation occured successfully, the products were generally a mixture of ethyl 3-, 5-, and 7-acylindole-2-carboxylates (4,5 and 6).The ratio of the yields of these three products varied greatly depending on reaction conditions and reagents used.A tendency that the 3-acylindole (4) was obtained as a main product was observed when a Lewis acid other than aluminum chloride was used as a catalyst and/or an acyl chloride derived from a weaker acid was employed, whereas a tendency for formation of the 5- and 7-acylindoles (5 and 6) was observed when aluminum chloride and/or an acyl chloride derived from a stronger acid was used.As to the 5- and 7-acylindoles (5 and 6) , the yields of the former were always much higher than those of the latter (6).The result indicates that ethyl 3- and 5-acylindole-2-carboxylates can be regioselectively prepared from a common substrate (1a) by changing the reaction conditions or reagents. friedel-craft acylation; ethyl indole-2-carboxylate; acyl chloride; acid anhydride; lewis acid; aluminum chloride; acylindole