56472-72-1

Basic information

• Product Name: 1-(4-chlorophenyl)propane-1,2-dione 2-oxime
• CAS NO: 56472-72-1
• Molecular Formula: C₉H₈ClNO₂
• Molecular Weight: 197.6183
• Mol File: 56472-72-1.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 339.2°C at 760 mmHg
• Flash Point: 159°C
• Density: 1.26g/cm³
• Vapor Pressure: 3.62E-05mmHg at 25°C
• Refractive Index: 1.559
• CAS DataBase Reference: 1-(4-chlorophenyl)propane-1,2-dione 2-oxime(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)propane-1,2-dione 2-oxime(56472-72-1)
• EPA Substance Registry System: 1-(4-chlorophenyl)propane-1,2-dione 2-oxime(56472-72-1)

Safety Data

• Hazardous Substances Data: 56472-72-1(Hazardous Substances Data)

Usage

Description

1-(4-chlorophenyl)propane-1,2-dione 2-oxime is a chemical compound belonging to the oxime class of organic compounds. It is derived from 1-(4-chlorophenyl)propane-1,2-dione, a ketone compound, with the addition of an oxime group. 1-(4-chlorophenyl)propane-1,2-dione 2-oxime's potential applications in various industrial and scientific processes are not well-documented, but its chemical structure suggests possible relevance in fields such as organic synthesis, pharmaceuticals, and material science. Further research is required to fully understand its characteristics and potential uses.

Uses

Used in Organic Synthesis:
1-(4-chlorophenyl)propane-1,2-dione 2-oxime is used as an intermediate in the synthesis of various organic compounds due to its unique chemical structure and reactivity.
Used in Pharmaceutical Industry:
1-(4-chlorophenyl)propane-1,2-dione 2-oxime is used as a potential building block for the development of new pharmaceuticals, given its structural features that may offer novel properties and activities.
Used in Material Science:
1-(4-chlorophenyl)propane-1,2-dione 2-oxime may be utilized as a component in the development of new materials, possibly due to its potential to influence the properties of the resulting materials.
(Note: The uses listed are speculative based on the compound's classification and structure. Actual applications may vary and require further investigation and validation through research and experimentation.)

Upstream product

• 6285-05-8 4'-chloropropiophenone 
• 544-16-1 n-Butyl nitrite 
• 123979-03-3 1-(p-Chlorphenyl)-2-methyl-glyoxim 
• 108-90-7 chlorobenzene 

Downstream Products

• 139325-73-8 4-[5-(4-Chloro-phenyl)-4-methyl-3-oxy-imidazol-1-yl]-2-hydroxy-benzoic acid 
• 10557-21-8 1-(4-chlorophenyl)propane-1,2-dione 
• 70071-22-6 2-(4-chlorophenyl)-3-methylquinoxaline 
• 123979-03-3 1-(4-chlorophenyl)-1,2-propanedione dioxime 
• 78587-05-0 N-cyclohexyl-(4RS,5RS)-5-(4-chlorophenyl)-4-methyl-2-oxo-1,3-thiazolidine-3-carboxamide 
• 23184-97-6 2-amino-1-(4-chlorophenyl)-1-propanone hydrochloride 

Relevant articles and documents

Dual photoredox/palladium-catalyzed C-H acylation of 2-arylpyridines with oxime esters

An unprecedented dual photoredox/palladium-catalyzed iminyl-radical-mediated C-C bond cleavage and directed ortho C-H acylation of 2-arylpyridines by using oxime esters is described. Oxime esters can serve as efficient acyl sources through formation of the corresponding acyl radicals by photoredox-catalyzed iminyl-radical-mediated C-C bond cleavage. This redox-neutral protocol features excellent regioselectivity, a broad substrate scope, and good functional-group tolerance with respect to both components, giving a broad range of aryl ketones with generally good yields.

An in vivo active 1,2,5-oxadiazole Pt(II) complex: A promising anticancer agent endowed with STAT3 inhibitory properties

New Pt(II) complexes (Pt-1-3) bearing 1,2,5-oxadiazole ligands (1-3) were synthesized, characterized and evaluated for their ability to disrupt STAT3 dimerization. Ligand 3·HCl showed cytotoxic effects on HCT-116 cells (IC50 = 95.2 μM) and a se

Reaction of Z isomers of alkylaromatic 1,2-hydroxylamino oximes with 1,2-diketones

The reactions of Z isomers of alkylaromatic 1,2-hydroxylamino oximes containing the hydroxylamino group at the primary or secondary carbon atom with diacetyl afford 6-acetyl-5,6-dihydro-4H-1,2,5-oxadiazines. The reactions of these compounds with alkylaromatic 1,2-diketones produce N-substituted α-aroylnitrones or 6-aroyl-5,6-dihydro-4H-1,2,5-oxadiazines or, alternatively, their tautomeric mixtures.