59146-66-6 Usage
Description
6-Ethylpicolinonitrile is a chemical compound with the molecular formula C8H8N2, classified as a nitrile. It is a versatile building block in organic synthesis, particularly in the production of pharmaceutical intermediates. Its unique structure and properties make it a valuable precursor for the synthesis of various functionalized compounds. Additionally, 6-Ethylpicolinonitrile has potential applications in the development of new materials with specialized properties. It is important to handle this compound with care, as it may pose health and environmental risks if not properly managed.
Uses
Used in Pharmaceutical Industry:
6-Ethylpicolinonitrile is used as a building block for the synthesis of pharmaceutical intermediates, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
6-Ethylpicolinonitrile is used as a precursor in the production of agrochemicals, aiding in the development of new pesticides and other agricultural chemicals.
Used in Organic Synthesis:
6-Ethylpicolinonitrile is used as a versatile building block in organic synthesis, enabling the creation of various functionalized compounds for different applications.
Used in Material Science:
6-Ethylpicolinonitrile is used in the development of new materials with specialized properties, potentially contributing to advances in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 59146-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,1,4 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 59146-66:
(7*5)+(6*9)+(5*1)+(4*4)+(3*6)+(2*6)+(1*6)=146
146 % 10 = 6
So 59146-66-6 is a valid CAS Registry Number.
59146-66-6Relevant articles and documents
Enantioselective Ni-Catalyzed Electrochemical Synthesis of Biaryl Atropisomers
Chen, Song,Chen, Yue-Gang,Gao, Pei-Sen,Liu, Dong,Ma, Hong-Xing,Mei, Tian-Sheng,Qiu, Hui,Shuai, Bin,Wang, Yun-Zhao
, p. 9872 - 9878 (2020/06/27)
A scalable enantioselective nickel-catalyzed electrochemical reductive homocoupling of aryl bromides has been developed, affording enantioenriched axially chiral biaryls in good yield under mild conditions using electricity as a reductant in an undivided cell. Common metal reductants such as Mn or Zn powder resulted in significantly lower yields in the absence of electric current under otherwise identical conditions, underscoring the enhanced reactivity provided by the combination of transition metal catalysis and electrochemistry.
QSAR in a series of muscarinic agents. Note IV. New pyridine and furan derivatives
Pratesi,Villa,Ferri,De Micheli,Grana,Santagostino Barbone,Silipo,Vittoria
, p. 398 - 410 (2007/10/02)
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