2157-58-6 Usage
Uses
Used in Organic Synthesis:
(NE)-N-(3,5,5-trimethyl-1-cyclohex-2-enylidene)hydroxylamine is used as a reagent for the preparation of various heterocyclic compounds, contributing to the diversity and complexity of organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (NE)-N-(3,5,5-trimethyl-1-cyclohex-2-enylidene)hydroxylamine serves as a building block for the synthesis of potential drug candidates, highlighting its importance in drug discovery and development.
Used in Medicinal Chemistry Research:
(NE)-N-(3,5,5-trimethyl-1-cyclohex-2-enylidene)hydroxylamine is used as a subject of interest in medicinal chemistry research due to its potential anti-inflammatory and anti-cancer properties, which could lead to the development of novel therapeutic agents.
Overall, (NE)-N-(3,5,5-trimethyl-1-cyclohex-2-enylidene)hydroxylamine is a valuable chemical compound with applications in organic synthesis, pharmaceuticals, and medicinal chemistry research, showcasing its potential in various fields of science and industry.
Check Digit Verification of cas no
The CAS Registry Mumber 2157-58-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 7 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2157-58:
(6*2)+(5*1)+(4*5)+(3*7)+(2*5)+(1*8)=76
76 % 10 = 6
So 2157-58-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H15NO/c1-7-4-8(10-11)6-9(2,3)5-7/h4,11H,5-6H2,1-3H3/b10-8-
2157-58-6Relevant academic research and scientific papers
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.
STEREOSELECTIVE ROUTE TO N-METHYL-2,3-CIS-DISUBSTITUTED PIPERIDINES
Neeson, S. J.,Stevenson, P. J.
, p. 3993 - 3996 (2007/10/02)
A new stereo-selective route to cis-disubstituted piperidines is presented in which the key step is a Stevens rearrangement with ring contraction.
