1188-63-2 Usage
Description
4-Heptanone oxime, with the chemical formula C7H15NO, is an oxime derivative of 4-heptanone. It is a versatile chemical compound that serves as a solvent and intermediate in the production of pharmaceuticals and other organic compounds. Known for its ability to inhibit the formation of advanced glycation end products, 4-heptanone oxime is a significant player in the realm of organic and pharmaceutical chemistry.
Uses
Used in Organic Synthesis:
4-Heptanone oxime is used as a reagent in chemical reactions for the synthesis of various organic compounds. Its unique properties make it a valuable component in creating a wide range of chemical products.
Used in Pharmaceutical Production:
As an intermediate in the production of pharmaceuticals, 4-heptanone oxime plays a crucial role in the development of new drugs and medicines. Its involvement in the synthesis process is essential for creating effective and safe pharmaceuticals.
Used in Inhibition of Advanced Glycation End Products:
4-Heptanone oxime is used as an inhibitor to prevent the formation of advanced glycation end products, which are associated with aging and various diseases. Its ability to inhibit these end products makes it a potential candidate for use in treatments targeting age-related conditions and diseases.
Used in Controlled Environments:
Due to its potential reactivity and toxicity, 4-heptanone oxime is typically handled and stored in a controlled environment. This ensures the safety of those working with the compound and minimizes the risk of adverse reactions or accidents.
Check Digit Verification of cas no
The CAS Registry Mumber 1188-63-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,8 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1188-63:
(6*1)+(5*1)+(4*8)+(3*8)+(2*6)+(1*3)=82
82 % 10 = 2
So 1188-63-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H15NO/c1-3-5-7(8-9)6-4-2/h9H,3-6H2,1-2H3
1188-63-2Relevant articles and documents
Selective Production of Hydrazine by a Catalytic Oxidation Process over Ti-, V-, Ti-V- and Ti-B-Silicalites
Kapoor, M. P.,Gallot, J. E.,Raj, A.,Kaliaguine, S.
, p. 2281 - 2282 (1995)
A simple catalytic process to obtain hydrazine by oxidation of ketone-NH3 system by H2O2 is reported; Ti-, V-, Ti-V- and Ti-B-silicalites of MFI structure are found to be active as catalysts in this oxidation reaction.
Copper-catalyzed synthesis of thiazol-2-yl ethers from oxime acetates and xanthates under redox-neutral conditions
Zhu, Zhongzhi,Tang, Xiaodong,Cen, Jinghe,Li, Jianxiao,Wu, Wanqing,Jiang, Huanfeng
supporting information, p. 3767 - 3770 (2018/04/17)
A novel copper-catalyzed annulation of oxime acetates and xanthates for the synthesis of thiazol-2-yl ethers with remarkable regioselectivity has been developed. Various oxime acetates, whether derived from aryl ketones or alkyl ketones, or natural product cores are suitable for this conversion. Unique dihydrothiazoles were also obtained when both reaction sites were methine. Mechanistic studies indicated that imino copper(iii) intermediates were involved. In addition, this protocol proceeded under redox-neutral conditions and did not require additives or ligands.
A mild synthesis of vinyl halides and gem-dihalides using triphenyl phosphite-halogen-based reagents
Spaggiari, Alberto,Vaccari, Daniele,Davoli, Paolo,Torre, Giovanni,Prati, Fabio
, p. 2216 - 2219 (2007/10/03)
A new application of (PhO)3P-halogen-based reagents to the synthesis of vinyl halides and gem-dihalides is described. Vinyl halides were prepared in good to excellent yields from enolizable ketones, whereas aldehydes afforded the corresponding gem-dihalides. The halogenation proceeded smoothly under mild conditions.