80935-81-5 Usage
Uses
Used in Pharmaceutical Synthesis:
2,6-Naphthyridin-1-amine(9CI) is utilized as a key building block in the creation of various pharmaceuticals and biologically active molecules. Its unique structure allows for the development of compounds with specific therapeutic properties, making it a valuable component in medicinal chemistry.
Used in Therapeutic Applications:
2,6-Naphthyridin-1-amine(9CI) has been studied for its potential as a therapeutic agent in the treatment of various diseases. Its specific biological activity and interaction with molecular targets make it a promising candidate for further research and development in the medical field.
Used in Material and Dye Development:
2,6-Naphthyridin-1-amine(9CI) has demonstrated its versatility in the development of new materials and dyes. Its chemical properties and structural features contribute to the creation of innovative products in the chemical and materials industries, enhancing their performance and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 80935-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,3 and 5 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80935-81:
(7*8)+(6*0)+(5*9)+(4*3)+(3*5)+(2*8)+(1*1)=145
145 % 10 = 5
So 80935-81-5 is a valid CAS Registry Number.
80935-81-5Relevant academic research and scientific papers
4-Piperidinecarboxamide modulators of vanilloid VR1 receptor
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Page/Page column 55, (2010/11/08)
This invention is directed to vanilloid receptor VR1 ligands. More particularly, this invention relates to hetero isonipecotic amides that are potent modulators of VR1 which are useful for the treatment and prevention of disease conditions in mammals.
Occurrence of Even Telesubstitution in the Amination of Halogeno-2,6-naphthyridines
Haak, Henk J. W. van den,Plas, Henk C. van der
, p. 1673 - 1677 (2007/10/02)
The conversion of 1-halogeno-2,6-naphthyridines into 1-amino-2,6-naphthyridine is shown to proceed via an even telesubstitution process N(AE)tele process>.The amination of 2-bromo-1,5-naphthyridine into 2-amino-1,5-naphthyridine is shown to proceed via an SN(AE)ipso substitution mechanism.
Amination of 2,6- and 2,7-Naphtyridine. An NMR Study on ?-Adducts of Heterocyclic Systems with Amide Ions
Haak, Henk J. W. van den,Plas, Henk C. van der,Veldhuizen, Beb van
, p. 1349 - 1352 (2007/10/02)
A facile synthesis of 2,6-naphtyridine is described.Both 2,6- and 2,7-naphtyridine undergo with potassium amide under kinetically and thermodynamically controlled conditions ?-adduct formation at position 1.Chichibabin amination of 2,6-naphtyridine yields 1-amino-2,6-naphtyridine in 54percent yield.
