829-08-3 Usage
Description
(1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime is a chemical compound with the molecular formula C10H13NO2. It is an oxime derivative of 2-hydroxy-2-methyl-1-phenylpropan-1-one, with the oxime group (-NOH) attached to the carbonyl carbon of the ketone. (1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime has potential applications in organic synthesis and medicinal chemistry.
Uses
Used in Organic Synthesis:
(1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime is used as a reagent for the preparation of various derivatives. Its unique structure allows for the synthesis of a range of organic compounds, making it a valuable building block in the development of new chemical entities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime serves as a building block in the synthesis of pharmaceutical compounds. Its ability to form various derivatives makes it a promising candidate for the development of new drugs with potential therapeutic applications.
Used in Pharmaceutical Research:
Oximes, including (1Z)-2-hydroxy-2-methyl-1-phenylpropan-1-one oxime, have been studied for their potential antioxidant and neuroprotective properties. This makes the compound a potentially valuable asset in pharmaceutical research, particularly for the development of treatments targeting oxidative stress-related conditions and neurodegenerative diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 829-08-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 9 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 829-08:
(5*8)+(4*2)+(3*9)+(2*0)+(1*8)=83
83 % 10 = 3
So 829-08-3 is a valid CAS Registry Number.
829-08-3Relevant articles and documents
Copper-Catalyzed Unstrained C-C Single Bond Cleavage of Acyclic Oxime Acetates Using Air: An Internal Oxidant-Triggered Strategy toward Nitriles and Ketones
Zhu, Chuanle,Chen, Fulin,Liu, Chi,Zeng, Hao,Yang, Zhiyi,Wu, Wanqing,Jiang, Huanfeng
, p. 14713 - 14722 (2018/12/14)
A copper-catalyzed aerobic oxidative C-C single bond cleavage of acyclic unstrained oxime acetates is reported, providing various aryl nitriles and ketones in good yields. Mechanistic studies indicate a radical procedure is involved in this transformation, and the oxygen atom in the ketone products is originated from O2 in the air. Oxime acetates as an internal oxidant have been proved to be an initiator, which may promote the discovery of novel protocol for C-C bond cleavage and dioxygen activation.
