6134-79-8

Basic information

• Product Name: 2,4-DIHYDROXYACETOPHENONE OXIME
• Synonyms: 2,4-DIHYDROXYACETOPHENONE OXIME;RESACETOPHENONE OXIME;(1E)-1-(2,4-dihydroxyphenyl)ethanone oxime;1-(2,4-Dihydroxyphenyl)ethanone oxime;4-[1-(Hydroxyimino)ethyl]benzene-1,3-diol
• CAS NO: 6134-79-8
• Molecular Formula: C₈H₉NO₃
• Molecular Weight: 167.16
• Product Categories: Aromatic Hydrazides, Hydrazines, Hydrazones and Oximes
• Mol File: 6134-79-8.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 384.4 °C at 760 mmHg
• Flash Point: 244.8 °C
• Appearance: /
• Density: 1.3 g/cm³
• Vapor Pressure: 0.000357mmHg at 25°C
• Refractive Index: 1.653
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,4-DIHYDROXYACETOPHENONE OXIME(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-DIHYDROXYACETOPHENONE OXIME(6134-79-8)
• EPA Substance Registry System: 2,4-DIHYDROXYACETOPHENONE OXIME(6134-79-8)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 6134-79-8(Hazardous Substances Data)

Usage

General Description

2,4-Dihydroxyacetophenone oxime, also known as acetophenone oxime, is a chemical compound with the molecular formula C8H9NO2. It is a white solid substance that is used as a chelating agent in various industries, including the manufacturing of pharmaceuticals, dyes, and rubber products. The compound is also used in analytical chemistry as a reagent for the determination of trace metals. It has the ability to form stable complexes with metal ions, making it useful in a variety of applications. Additionally, 2,4-dihydroxyacetophenone oxime has been studied for its potential antioxidant and anti-inflammatory properties, showing promise for potential therapeutic use in the future.

InChI:InChI=1/C8H9NO3/c1-5(9-12)7-3-2-6(10)4-8(7)11/h2-4,9,11-12H,1H3/b7-5-

Upstream product

• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 5470-11-1 hydroxylamine hydrochloride 

Downstream Products

• 114594-14-8 C₁₄H₁₇NO₅ 
• 5078-07-9 6-hydroxy-2-methylbenzoxazole 
• 76288-39-6 7-hydroxy-3-phenyl-2,3-dihydro-1H-pyrido<1,2-b><1,2>benzisoxazole-1,2-dicarboxylic acid 
• 76288-35-2 8-Hydroxy-4-(4-methoxy-phenyl)-3a,10b-dihydro-4H-2,10-dioxa-10a-aza-cyclopenta[a]fluorene-1,3-dione 
• 76288-33-0 8-hydroxy-1,3-dioxo-4-phenyl-1,3a,4,10b-tetrahydro-2,10-dioxa-10a-aza-3H-cyclopentafluorene 
• 76288-27-2 3-[(E)-2-(4-Methoxy-phenyl)-vinyl]-benzo[d]isoxazol-6-ol 
• 76288-25-0 6-hydroxy-3-styryl-1,2-benzisoxazole 
• 66033-92-9 6-hydroxy-3-methyl-1,2-benzisoxazole 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 49586-28-9 1-(4-acetoxy-2-hydroxy-phenyl)-ethanone O-acetyl-oxime 
• 69658-70-4 1-(2,4-dihydroxy-phenyl)-ethanon-(O-acetyl oxime ) 

Relevant articles and documents

Structures and magnetism of two manganese crowns assembled with 2,4-dihydroxyacetophenone oxime

Reactions of 2,4-dihydroxyacetophenone oxime with manganese salts yielded two manganese crowns, [Mn3(μ3-O)(4-OH-Me-sao) 3(HCOO)(MeOH)5].MeOH (1) and [Mn3(μ 3-O)(4-OH-Mesao) 3(CH3

Benzoisoxazole compound derivative and applications thereof

The present invention provides a benzoisoxazole compound derivative and applications thereof. According to the present invention, the in vitro receptor binding assay results show that the compound hashigh affinity to H3 receptors, can be used for improvin

Natural products as sources of new fungicides (II): antiphytopathogenic activity of 2,4-dihydroxyphenyl ethanone derivatives

A series of 17 simple 1-(2,4-dihydroxyphenyl) ethanones were synthesised, and their structures characterised by 1H, 13C NMR and ESI-MS. Their in vitro antifungal activities were evaluated against five phytopathogenic fungi including Glomerella cingulate, Botrytis cirerea, Fusarium graminearum, Curvularia lunata and Fusarium oxysporum f. sp. vasinfectum by the mycelial growth inhibition assay. Compounds 2g and 2h exhibited broad-spectrum inhibitory activity against the mycelial growth of the tested pathogens with IC50 values in the range of 16-36 g/mL, and in particular being more active to G. cingulate, with IC50 values of 16.50 and 19.25 g/mL, respectively, than the other pathogens. Preliminary SAR indicated that an α,β-unsaturated ketone unit of the alkyl chain of the compounds is the structure requirement for fungicidal action. The results suggested that 2g and 2h may be promising leads in the development of new antifungal agents.