17512-70-8 Usage
Description
2-fluoro-N-hydroxybenzamide is a chemical compound characterized by the molecular formula C7H6FNO2. It is a benzamide derivative featuring a fluorine atom and a hydroxyl group attached to the benzene ring. 2-fluoro-N-hydroxybenzamide is recognized for its potential in organic synthesis and pharmaceutical research, where it serves as a versatile building block for the creation of novel chemical structures. The unique structural attributes of 2-fluoro-N-hydroxybenzamide have positioned it as a promising candidate for exploring new avenues in drug development and chemical processes.
Uses
Used in Organic Synthesis:
2-fluoro-N-hydroxybenzamide is utilized as a key intermediate in organic synthesis for the construction of complex organic molecules. Its presence of a fluorine atom and hydroxyl group on the benzene ring allows for a variety of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-fluoro-N-hydroxybenzamide is employed as a starting material for the development of new drugs. Its unique structure and properties make it a candidate for the design of innovative therapeutic agents. Researchers are investigating its potential biological activities, which may lead to the discovery of new treatments for various diseases.
Used in Drug Development:
2-fluoro-N-hydroxybenzamide may have implications in the development of new medications due to its distinct structural features. Its ability to be modified and incorporated into diverse chemical frameworks positions it as a promising scaffold for the creation of novel drug candidates with potential therapeutic benefits.
Used in Chemical Processes:
2-fluoro-N-hydroxybenzamide's unique structure and reactivity also make it suitable for use in various chemical processes. It can be employed to improve the efficiency of chemical reactions, develop new synthetic routes, and enhance the properties of existing materials.
Check Digit Verification of cas no
The CAS Registry Mumber 17512-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,5,1 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17512-70:
(7*1)+(6*7)+(5*5)+(4*1)+(3*2)+(2*7)+(1*0)=98
98 % 10 = 8
So 17512-70-8 is a valid CAS Registry Number.
17512-70-8Relevant articles and documents
A new method for preparing N-acyloxaziridines via tandem O, N-addition of hydroxamic acids to methyl propiolate.
Zong, Kyukwan,Shin, Seung Il,Ryu, Eung Kul
, p. 6227 - 6228 (1998)
N-Acyloxaziridines were prepared from a tandem O, N-addition of hydroxamic acids to metyl propiolate in the presence of 4-methyl morpholine as a catalyst in good to excellent yields.
Rhodium(III)-catalyzed C4-amidation of indole-oximes with dioxazolones: Via C-H activation
Deng, Ke-Zuan,Fu, Xiao-Pan,Ji, Ya-Fei,Tang, Shi-Biao,Wu, Gao-Rong,Xia, Cheng-Cai,Yang, Jin-Yue,Zhang, Li-Li
supporting information, p. 7922 - 7931 (2020/11/02)
A novel method for the Rh(III)-catalyzed oxime-directed C-H amidation of indoles with dioxazolones has been developed. This strategy provides an exclusive site selectivity and the directing group can be easily removed. This transformation features a wide substrate scope, good functional group tolerance and excellent yields, and may serve as a significant tool to construct structurally diverse indole derivatives for the screening of potential pharmaceuticals in the future. This journal is
Synthesis of 2,5-disubstituted oxazoles: Via cobalt(III)-catalyzed cross-coupling of N -pivaloyloxyamides and alkynes
Yu, Xiaolong,Chen, Kehao,Wang, Qi,Zhang, Wenjing,Zhu, Jin
supporting information, p. 1197 - 1200 (2018/02/09)
An efficient synthesis of 2,5-disubstituted oxazoles via Co(iii) catalysis is described herein. The synthesis is achieved under mild conditions through [3+2] cycloaddition of N-pivaloyloxyamides and alkynes. The reaction operates through an internal oxidation pathway and features a very broad substrate scope. The one-step synthesis of natural products such as texamine and balsoxin has been demonstrated via this protocol.
