51864-09-6

Basic information

• Product Name: 1-(1-Hydroxy-2-naphtyl)ethanone oxime
• Synonyms: 1-(1-Hydroxy-2-naphthalenyl)ethanone oxime;1-(1-Hydroxy-2-naphtyl)ethanone oxime
• CAS NO: 51864-09-6
• Molecular Formula: C₁₂H₁₁NO₂
• Molecular Weight: 201.2212
• Mol File: 51864-09-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 380.3°Cat760mmHg
• Flash Point: 183.8°C
• Appearance: /
• Density: 1.275g/cm³
• Vapor Pressure: 1.85E-06mmHg at 25°C
• Refractive Index: 1.638
• CAS DataBase Reference: 1-(1-Hydroxy-2-naphtyl)ethanone oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-Hydroxy-2-naphtyl)ethanone oxime(51864-09-6)
• EPA Substance Registry System: 1-(1-Hydroxy-2-naphtyl)ethanone oxime(51864-09-6)

Safety Data

• Hazardous Substances Data: 51864-09-6(Hazardous Substances Data)

Usage

General Description

1-(1-Hydroxy-2-naphthyl)ethanone oxime is a chemical compound with the molecular formula C12H11NO2. It is an oxime derivative of 1-(1-hydroxy-2-naphthyl)ethanone, and is commonly used in organic synthesis and biochemical research. The compound is known to possess antioxidant properties and has been studied for its potential therapeutic applications, particularly in the treatment of oxidative stress-related disorders. It is also used as a chelating agent in the complexation of metal ions, and is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals. Overall, 1-(1-Hydroxy-2-naphthyl)ethanone oxime is a versatile compound with diverse applications in scientific research and industrial processes.

InChI:InChI=1/C12H11NO2/c1-8(13-15)10-7-6-9-4-2-3-5-11(9)12(10)14/h2-7,13,15H,1H3/b10-8+

Upstream product

• 574-19-6 1-(2-hydroxy-1-naphthyl)ethan-1-one 
• 90-15-3 α-naphthol 
• 711-79-5 1-hydroxy-2-acetonaphthone 

Downstream Products

• 20686-65-1 2-methyloxazolo<4,5-a>naphthalene 
• 76288-32-9 C₄₁H₃₀N₂O₄ 
• 76288-31-8 C₃₉H₂₆N₂O₂ 
• 76288-38-5 4-(4-Methoxy-phenyl)-3a,12b-dihydro-4H-2,12-dioxa-12a-aza-benzo[a]cyclopenta[i]fluorene-1,3-dione 
• 76288-40-9 3-phenyl-2,3-dihydro-1H-pyrido<1,2-b>benzo<1,2>benzisoxazole-1,2-dicarboxylic acid 
• 76288-37-4 1,3-dioxo-4-phenyl-1,3a,4,12b-tetrahydro-2,12-dioxa-12a-aza-3H-cyclopentabenzofluorene 
• 76288-30-7 3-[(E)-2-(4-Methoxy-phenyl)-vinyl]-naphtho[2,1-d]oxazole 
• 76288-29-4 3-styrylnaphth<2,1-d>isoxazole 

Relevant articles and documents

Cube-like 12-MC-4 and Offset Stacked 10-MC-3 Metallacrowns: Synthesis, Structure, and Magnetic Properties

Two complexes [MnIII4(naphthsao)4(naphthsaoH)4] (1) and [FeIII6O2(naphthsao)4(O2CPh)6] (2) [naphthsao = 1-(1-hydroxy-naphthalen-2-yl)ethanone oxi

Synthesis of New Isoxazoles from Isoxazolines, Chalkones, Chalkone Dibromides, Epoxides and Acetylated Ketoximes and Their Conversion into Novel Heterocycles

A convenient and easy conversion of 2-isoxazolines (II) to isoxazoles (V) via N-bromosuccinimide bromination and subsequent dehydrobromination with bases is described.The isoxazoles have also been synthesized from chalkones (I), chalkone dibromides (III)