6994-14-5 Usage
Uses
Used in Pharmaceutical Research and Manufacturing:
N-(1-Oxidopyridin-2-yl)acetamide is used as a building block for the synthesis of various bioactive compounds, contributing to the development of new pharmaceuticals with potential therapeutic applications.
Used in the Synthesis of Heterocyclic Compounds:
N-(1-Oxidopyridin-2-yl)acetamide is utilized as a key intermediate in the synthesis of heterocyclic compounds, which are important in various chemical and pharmaceutical applications due to their diverse chemical properties and biological activities.
Used in Agrochemical Production:
N-(1-Oxidopyridin-2-yl)acetamide is employed in the production of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals that help protect crops and enhance agricultural productivity.
Check Digit Verification of cas no
The CAS Registry Mumber 6994-14-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,9 and 4 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6994-14:
(6*6)+(5*9)+(4*9)+(3*4)+(2*1)+(1*4)=135
135 % 10 = 5
So 6994-14-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-6(10)8-7-4-2-3-5-9(7)11/h2-5,11H,1H3/b8-7+
6994-14-5Relevant academic research and scientific papers
A new transformation of aminopyridines upon diazotization in acetonitrile with the formation of N-pyridinylacetamides
Chudinov,Dovbnya,Krasnokutskaya,Ogorodnikov,Filimonova
, p. 2312 - 2314 (2017/05/12)
Diazotization of aminopyridines upon treatment with NaNO2 and H3PO4 in acetonitrile led to the formation of N-pyridinylacetamides. This reaction constitutes a convenient and general preparative method for the synthesis of 2-, 3-, and 4-N-pyridinylacetamides under mild conditions in good yields. The in situ oxidation of the thus obtained N-pyridinylacetamides with hydrogen peroxide gave good yields of pyridinylacetamide N-oxides.
Self-assembly of organocatalysts: Fine-tuning organocatalytic reactions
Clarke, Matthew L.,Fuentes, Jose A.
, p. 930 - 933 (2008/02/01)
(Chemical Equation Presented) A cat. with two tales: Hydrogen-bonding interactions between achiral pyridinone additives and unselective chiral proline-derived organocatalysts (see picture) result in highly effective catalysts for the Michael addition of n
