16232-41-0 Usage
Description
3-Cyano-2-hydroxy-6-methyl-4-phenylpyridine is a pyridine derivative with the molecular formula C13H10N2O. It features a cyano group, a hydroxy group, a methyl group, and a phenyl group attached to the pyridine ring. This synthetic intermediate is widely used in the production of pharmaceuticals, agrochemicals, and other organic compounds. Due to its potential biological activity, it serves as a valuable building block in the synthesis of various functional materials. However, it is considered hazardous if ingested or inhaled, necessitating appropriate safety measures during handling.
Uses
Used in Pharmaceutical Industry:
3-Cyano-2-hydroxy-6-methyl-4-phenylpyridine is used as a synthetic intermediate for the development of pharmaceuticals. Its unique structure allows it to be a key component in the synthesis of various drugs, contributing to their therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 3-Cyano-2-hydroxy-6-methyl-4-phenylpyridine is utilized as a building block in the creation of agrochemicals. Its incorporation into these compounds can enhance their effectiveness in agricultural applications, such as pest control and crop protection.
Used in Organic Compounds Synthesis:
3-Cyano-2-hydroxy-6-methyl-4-phenylpyridine is employed as a synthetic intermediate in the synthesis of various organic compounds. Its versatile structure makes it a valuable component in the development of new materials with specific properties and functions.
Used in Functional Materials Development:
Due to its potential biological activity, 3-Cyano-2-hydroxy-6-methyl-4-phenylpyridine is used as a building block in the development of functional materials. Its incorporation into these materials can impart unique characteristics, making them suitable for various applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 16232-41-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,2,3 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 16232-41:
(7*1)+(6*6)+(5*2)+(4*3)+(3*2)+(2*4)+(1*1)=80
80 % 10 = 0
So 16232-41-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H10N2O/c1-9-7-11(10-5-3-2-4-6-10)12(8-14)13(16)15-9/h2-7H,1H3,(H,15,16)
16232-41-0Relevant articles and documents
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Bomika et al.
, (1975)
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Synthesis and Photophysical Properties of 3-Amino-4-arylpyridin-2(1 H)-ones
Abramov, Anton A.,Chernenko, Sergey A.,Fisyuk, Alexander S.,Kostyuchenko, Anastasia S.,Shatsauskas, Anton L.
, p. 227 - 238 (2019/12/28)
A method has been developed for the preparation of oxazolo-[5,4- b ]pyridin-2(1 H)-ones based on the Hoffmann reaction of 2-oxo-1,2-dihydropyridine-3-carboxamides. Hydrolysis of oxazolo[5,4- b ]pyridin-2(1 H)-ones and the Hoffmann reaction of 2-oxo-1,2-dihydropyridine-3-carboxamides yielded 3-aminopyridin-2(1 H)-ones, including 4-aryl substituted derivatives in the series, for which effective phosphors with a quantum yield of up to 0.78 were detected. Photophysical properties of 3-aminopyridin-2(1 H)-ones were studied by UV and luminescence spectroscopy methods, and the relationship between their structure and photophysical properties was revealed.
One-Pot Synthesis of 3-Cyano-2-pyridones
Wang, Yingcai,Liu, Gang,Reyes, Jeremy Chris P.,Duverna, Randolph
, p. 1185 - 1191 (2015/08/06)
A versatile synthesis of 3-cyano-2-pyridones via a one-pot, four-component condensation of ethyl cyanoacetate, ketones, aldehydes, and ammonium acetate under very mild conditions has been developed. This method provides rapid access to this type of valuab
AZAINDAZOLES
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Page/Page column 53; 54, (2013/03/28)
Herein are disclosed azaindazoles of formula (I), (I), where the various groups are defined herein, and which are useful for treating cancer.
