130875-68-2 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The systematic name provides a standardized way to name the compound based on its structure and functional groups.
Explanation
Naphthyridine Oximes are a group of organic compounds containing a naphthyridine moiety, which is a tricyclic aromatic compound made up of a benzene ring fused to a pyridine ring.
Explanation
The naphthyridine moiety is a key structural feature of the compound, consisting of a benzene ring fused to a pyridine ring.
Explanation
1,8-Naphthyridin-4(1H)-one,7-ethoxy-2,3-dihydro-,oxime,(Z)-(9CI) is not commonly found in nature and is usually created through chemical synthesis for specific uses in research and the pharmaceutical industry.
Explanation
The naphthyridine structure of the compound suggests that it may have potential applications in the fields of pharmacology and medical research, although its exact properties and uses have not been extensively documented.
Explanation
The specific properties, uses, and availability of 1,8-Naphthyridin-4(1H)-one,7-ethoxy-2,3-dihydro-,oxime,(Z)-(9CI) are not well-documented, indicating that it may be a relatively obscure or specialized compound.
Class
Naphthyridine Oximes
Structure
Contains a naphthyridine moiety
Synthesis
Typically synthesized for research and pharmaceutical applications
Potential Applications
Pharmacology and medical research
Availability
Not extensively documented
Check Digit Verification of cas no
The CAS Registry Mumber 130875-68-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,7 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 130875-68:
(8*1)+(7*3)+(6*0)+(5*8)+(4*7)+(3*5)+(2*6)+(1*8)=132
132 % 10 = 2
So 130875-68-2 is a valid CAS Registry Number.
130875-68-2Relevant academic research and scientific papers
Synthesis and β-blocking activity of (E)- and (Z)-iminoethers of 1,8-naphthyridine. Potential antihypertensive agents. 4
Ferrarini,Mori,Primofiore,Da Settimo,Breschi,Martinotti,Nieri,Ciucci
, p. 489 - 496 (2007/10/02)
A series of substituted (E)- and (Z)-iminoethers of 1,8-naphthyridine was synthesized from corresponding ketones. The pharmacological activity of these compounds was evaluated on isolated preparations to assess the eventual interaction with α and β adrenoceptors. All the compounds exhibited β2 stimulating and β1 blocking properties, while on α receptors neither stimulating nor blocking activity was observed.
