56472-73-2 Usage
Uses
Used in Organic Synthesis:
1-(4-bromophenyl)propane-1,2-dione 2-oxime is used as a building block in organic synthesis for the creation of various pharmaceuticals and bioactive compounds due to its versatile chemical structure and reactivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(4-bromophenyl)propane-1,2-dione 2-oxime is utilized as a key intermediate for the development of new drugs, taking advantage of its potential biological activities and synthetic utility.
Used in Pharmaceutical Industry:
1-(4-bromophenyl)propane-1,2-dione 2-oxime is used as a precursor in the pharmaceutical industry for the synthesis of drugs with potential applications in treating various diseases and conditions, leveraging its antioxidant and anti-inflammatory properties.
Used in Research and Development:
1-(4-bromophenyl)propane-1,2-dione 2-oxime is also used in research and development settings to study its potential use in the treatment of different diseases and conditions, as well as to explore its biological activities further.
Check Digit Verification of cas no
The CAS Registry Mumber 56472-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,7 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 56472-73:
(7*5)+(6*6)+(5*4)+(4*7)+(3*2)+(2*7)+(1*3)=142
142 % 10 = 2
So 56472-73-2 is a valid CAS Registry Number.
56472-73-2Relevant academic research and scientific papers
Dual photoredox/palladium-catalyzed C-H acylation of 2-arylpyridines with oxime esters
He, Bin-Qing,Gao, Yuan,Wang, Peng-Zi,Wu, Hong,Zhou, Hong-Bin,Liu, Xiao-Peng,Chen, Jia-Rong
supporting information, p. 373 - 377 (2020/09/11)
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.
Reaction of Z isomers of alkylaromatic 1,2-hydroxylamino oximes with 1,2-diketones
Amitina,Grigor'ev,Tikhonov
, p. 1046 - 1051 (2008/02/01)
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.
