142502-88-3 Usage
Description
2(1H)-Pyridinone,3-ethynyl-(9CI), also known as 3-Ethynylpyridin-2-ol, is an organic compound with a unique structure that features a pyridinone core and an ethynyl group. 2(1H)-Pyridinone,3-ethynyl-(9CI) is characterized by its potential reactivity and versatility in chemical synthesis, making it a valuable building block for various applications in the chemical and pharmaceutical industries.
Uses
Used in Chemical Synthesis:
2(1H)-Pyridinone,3-ethynyl-(9CI) is used as a reactant in the preparation and coupling reaction of ethynylpyridone subunits. Its ethynyl group allows for further functionalization and the formation of complex molecular structures, which can be utilized in the development of new compounds with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2(1H)-Pyridinone,3-ethynyl-(9CI) can be used as a key intermediate in the synthesis of various drug candidates. Its unique structure and reactivity enable the development of novel therapeutic agents with potential applications in treating different diseases and medical conditions.
Used in Material Science:
The compound's ethynyl group also makes it a candidate for use in the development of new materials with specific properties, such as conductivity, magnetism, or optical characteristics. These materials can find applications in various fields, including electronics, sensors, and energy storage devices.
Check Digit Verification of cas no
The CAS Registry Mumber 142502-88-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142502-88:
(8*1)+(7*4)+(6*2)+(5*5)+(4*0)+(3*2)+(2*8)+(1*8)=103
103 % 10 = 3
So 142502-88-3 is a valid CAS Registry Number.
142502-88-3Relevant articles and documents
Furopyridines. XXXI [1]. Birch reduction of furopyridines
Yamaguchi, Seiji,Hamade, Eriko,Yokoyama, Hajime,Hirai, Yoshiro,Shiotani, Shunsaku
, p. 335 - 339 (2007/10/03)
Birch reduction of four furopyridines 1a-d effected the characteristic cleavage of the furan ring, giving ethnylpyridinols 2a-d, vinylpyridinols 3b,d, and ethylpyridinols 4a-d, and the reduction of the furan ring, giving dihydrofuropyridine 5c,d.
