20151-01-3 Usage
Description
1-(4-nitrophenyl)-2-(pyridin-2-yl)ethanol is a chemical compound with a molecular formula C13H11NO3. It is a yellow crystalline solid that is a derivative of both phenol and pyridine, featuring a nitro group on the phenyl ring. 1-(4-nitrophenyl)-2-(pyridin-2-yl)ethanol has been studied for its potential biological activity, which includes possible anti-inflammatory and analgesic properties. Its unique structure also suggests potential applications in organic synthesis and as a reagent in chemical reactions. However, due to its potential hazardous properties, it should be handled with care and used in a controlled laboratory environment.
Uses
Used in Pharmaceutical Applications:
1-(4-nitrophenyl)-2-(pyridin-2-yl)ethanol is used as a potential pharmaceutical agent for its possible anti-inflammatory and analgesic properties. Its biological activity makes it a candidate for the development of new drugs targeting inflammation and pain.
Used in Organic Synthesis:
In the field of organic chemistry, 1-(4-nitrophenyl)-2-(pyridin-2-yl)ethanol is used as a reagent in various chemical reactions. Its unique structure allows it to participate in a range of synthetic processes, contributing to the creation of diverse chemical products.
Used in Chemical Research:
1-(4-nitrophenyl)-2-(pyridin-2-yl)ethanol is also utilized in chemical research as a model for studying the effects of structural modifications on the biological activity of phenol and pyridine derivatives. Understanding these effects can guide the design of more effective pharmaceutical drugs and other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 20151-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,5 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 20151-01:
(7*2)+(6*0)+(5*1)+(4*5)+(3*1)+(2*0)+(1*1)=43
43 % 10 = 3
So 20151-01-3 is a valid CAS Registry Number.
20151-01-3Relevant articles and documents
Magnetically separable CuFe2O4 nanoparticles as a recoverable catalyst for the addition reaction of C(sp3)-H bond of azaarenes to aldehydes
Wang, Zu-Li
, p. 5563 - 5566 (2015/03/05)
A green and efficient protocol for the copper ferrite (CuFe2O4) nanoparticle-catalyzed direct C(sp3)-H bond functionalization of 2-alkyl azaarenes has been developed. The magnetic catalyst can be recovered and recycled by a simple magnetic separation from the reaction solution and reused eight times without significant decrease in catalytic activity. This journal is
Acid ionic liquid promoted addition of C(sp3)-H bond to aldehyde
Zhang, Xue-Yan,Dong, Dao-Qing,Yue, Tao,Hao, Shuang-Hong,Wang, Zu-Li
supporting information, p. 5462 - 5464 (2014/12/11)
A novel protocol for acid ionic liquid promoted C(sp3)-H bond functionalization of alkyl azaarenes and nucleophilic addition to aldehydes was developed in good to excellent yields, which provides an efficient approach for the synthesis of alkyl-substituted azaarene derivatives. It is worthwhile to note that acid ionic liquid used for this reaction can be recycled and reused six times without a significant decrease in activity.
Bronsted acid promoted benzylic C-H bond functionalization of azaarenes: Nucleophilic addition to aldehydes
Wang, Fang-Fang,Luo, Cui-Ping,Wang, Yi,Deng, Guojun,Yang, Luo
supporting information, p. 8605 - 8608 (2013/01/15)
A practical Bronsted acid promoted benzylic C-H functionalization of 2-methylazaarenes and nucleophilic addition to aldehydes was developed in good to excellent yields. A six-membered hydrogen-bonding transition state is proposed to be crucial for the reaction. Ready availability of the two starting materials, the use of acetic acid as the catalyst and the facile reaction conditions will guarantee this synthetic method attractive to the synthesis of bioactive pyridine and quinoline derivatives.
