1007-18-7 Usage
Uses
Used in Pharmaceutical Synthesis:
N-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide is utilized as a key precursor in the development of pharmaceuticals. Its unique chemical properties and structural features allow for the creation of a variety of medicinal compounds, contributing to the advancement of drug discovery and therapeutic options.
Used in Organic Synthesis:
In the field of organic synthesis, N-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide serves as a versatile building block. Its ability to be modified and incorporated into more complex molecules makes it an essential component in the synthesis of a wide range of organic compounds, including those with potential applications in various industries.
Used in Research and Development:
Due to its potential pharmacological activity and structural similarity to other biologically active compounds, N-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide is employed in research and development settings. It is used to explore new chemical pathways, investigate its interactions with biological systems, and develop novel therapeutic agents.
Used in Chemical Intermediates Production:
As a chemical intermediate, N-methyl-6-oxo-1,6-dihydropyridine-3-carboxamide is used in the production of various chemical products. Its unique structure and reactivity make it suitable for the synthesis of a range of intermediates that are essential in the manufacturing process of different chemical and pharmaceutical products.
Check Digit Verification of cas no
The CAS Registry Mumber 1007-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,0 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1007-18:
(6*1)+(5*0)+(4*0)+(3*7)+(2*1)+(1*8)=37
37 % 10 = 7
So 1007-18-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2/c1-8-7(11)5-2-3-6(10)9-4-5/h2-4H,1H3,(H,8,11)(H,9,10)
1007-18-7Relevant academic research and scientific papers
Pyrimidines. 54. Ring Transformation of 5-(2-Carbamoylvinyl)uracil Derivatives to 5-Carbamoylpyridin-2-ones
Hirota, Kosaku,Kitade, Yukio,Shimada, Kaoru,Maki, Yoshifumi
, p. 1512 - 1516 (2007/10/02)
Reaction of 5-formyluracil derivatives 1 with (carbamoylmethylene)triphenylphosphorane led to the formation of both the corresponding (Z)- and (E)-5-(2-carbamoylvinyl)uracil derivatives 2 and 3.Upon treatment of the Z isomers 2 with ethanolic sodium ethoxide, a mononuclear heterocyclic rearrangement occurred easily to give 3-(ethoxycarbamoyl)pyridin-6-ones (4) and 3-(N-substituted carbamoyl)pyridin-6-ones (5).Under the analogous conditions, the E isomers 3 were converted into 4 and 5 together with 3-(N-substituted carbamoyl)-1-methylpyridin-6-ones (6).Addition of water to the reaction mixture accelerated the conversion of 3 into 6.Conceivable reaction sequences for the present pyrimidine-to-pyridine transformations are discussed.
