1219130-55-8 Usage
Uses
Used in Organic Synthesis:
2-pyridinone-8-boronic ester is used as a building block for the construction of various organic molecules due to its ability to undergo diverse chemical transformations. Its reactivity and selectivity make it a preferred choice for creating new and valuable chemical compounds.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-pyridinone-8-boronic ester is used as a key intermediate for the synthesis of potential drug candidates. Its versatile reactivity allows for the introduction of functional groups into organic molecules, facilitating the development of new therapeutic agents.
Used in Agrochemicals:
2-pyridinone-8-boronic ester is utilized in the agrochemical sector as a precursor for the synthesis of bioactive compounds with potential applications in pest control and crop protection. Its reactivity enables the creation of novel agrochemicals with improved efficacy and selectivity.
Used in Materials Science:
In the field of materials science, 2-pyridinone-8-boronic ester is employed as a component in the development of advanced materials with specific properties. Its ability to introduce functional groups into organic molecules contributes to the creation of materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 1219130-55-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,9,1,3 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1219130-55:
(9*1)+(8*2)+(7*1)+(6*9)+(5*1)+(4*3)+(3*0)+(2*5)+(1*5)=118
118 % 10 = 8
So 1219130-55-8 is a valid CAS Registry Number.
1219130-55-8Relevant articles and documents
5-HETEROARYL-PYRIDIN-2-AMINE CONFOUNDS AS NEUROPEPTIDE FF RECEPTOR ANTAGONISTS
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Page/Page column 75, (2021/02/12)
The present invention relates to novel aminopyridine derivatives of the general formula (I) and pharmaceutical compositions comprising these compounds, as well as their therapeutic use, particularly as neuropeptide FF (NPFF) receptor antagonists, including, e.g., for the treatment or prevention of pain, opioid-induced hyperalgesia, or addiction.
Noncovalent Interactions in Ir-Catalyzed C-H Activation: L-Shaped Ligand for Para-Selective Borylation of Aromatic Esters
Hoque, Md Emdadul,Bisht, Ranjana,Haldar, Chabush,Chattopadhyay, Buddhadeb
supporting information, p. 7745 - 7748 (2017/06/21)
An efficient strategy for the para-selective borylation of aromatic esters is described. For achieving high para-selectivity, a new catalytic system has been developed modifying the core structure of the bipyridine. It has been proposed that the L-shaped ligand is essential to recognize the functionality of the oxygen atom of the ester carbonyl group via noncovalent interaction, which provides an unprecedented controlling factor for para-selective C-H activation/borylation.
HETEROCYCLIC BIARYL DERIVATIVE AND PDE INHIBITOR COMPRISING SAME AS ACTIVE INGREDIENT
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Page/Page column 31, (2011/08/04)
Novel heterocyclic biaryl derivatives were disclosed which are useful as pharmaceutical agents and which exhibit a phosphodiesterase-inhibitory action. The heterocyclic biaryl derivatives are represented by the following general formula (1): wherein the H
