51420-73-6 Usage
General Description
The chemical compound 5,7-Bis(Trifluoromethyl)[1,8]Naphthyridin-2-ol is a specialized organic compound. Its name suggests that it contains two types of functional groups: the trifluoromethyl group, denoted by the (Trifluoromethyl) part of its name, and the naphthyridinol group, denoted by the [1,8]Naphthyridin-2-ol part of the name. Due to the nature of its structure, this compound is primarily used in research and development settings and is not typically found in household or common industrial products. The details of its behaviour, reactions, and potential use are usually expounded upon in scientific research and studies.
Check Digit Verification of cas no
The CAS Registry Mumber 51420-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51420-73:
(7*5)+(6*1)+(5*4)+(4*2)+(3*0)+(2*7)+(1*3)=86
86 % 10 = 6
So 51420-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H4F6N2O/c11-9(12,13)5-3-6(10(14,15)16)17-8-4(5)1-2-7(19)18-8/h1-3H,(H,17,18,19)
51420-73-6Relevant articles and documents
Polymorphic equilibrium responsive thermal and mechanical stimuli in light-emitting crystals of N -methylaminonaphthyridine
Harada, Naomi,Abe, Yuichiro,Karasawa, Satoru,Koga, Noboru
, p. 6282 - 6285 (2013/02/25)
Crystal polymorphs of 1,8-naphthyridine derivative, being anti and syn conformers, show a reversible transformation from anti to syn by heating and from syn to anti by grinding with the alteration of emittance intensity, and notably, thermal transformation from anti to syn conformer took place in single-crystal-to-single-crystal (SC-to-SC) form, which was confirmed by a single crystal X-ray crystallography.
1,8-Naphthyridine compounds
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, (2008/06/13)
There is described 2-amino-5,7-disubstituted-naphthyridine and 5,7-disubstituted-naphthyridin-2(1H)-one derivatives with bronchodilating and hypotensive properties prepared by the reaction of 2,6-diaminopyridine with an appropriate β-diketone providing the 2-amino products. The 2-oxo analogs are prepared from the 2-amino products by treatment with nitrous acid.
