75883-48-6 Usage
Chemical structure
A complex molecule with a piperidinium chloride structure, containing multiple functional groups.
Ethoxycarbonyl amino group
A functional group consisting of an ethoxycarbonyl (-COOEt) group attached to an amino (-NH2) group.
Multiple methoxy groups
The presence of more than one methoxy (-OCH3) group attached to a benzofuran ring.
Benzofuran ring
A heterocyclic aromatic ring consisting of a benzene ring fused to a furan ring.
Ethylenedioxypiperidine ring
A six-membered nitrogen-containing ring with two oxygen atoms in the 1,4-positions, forming an ethylenedioxy bridge.
Potential applications
The chemical structure may have potential applications in pharmacology, medicine, or industrial chemistry.
Further study required
Additional research and analysis are needed to determine the specific properties and potential uses of this molecule.
Check Digit Verification of cas no
The CAS Registry Mumber 75883-48-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,8,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75883-48:
(7*7)+(6*5)+(5*8)+(4*8)+(3*3)+(2*4)+(1*8)=176
176 % 10 = 6
So 75883-48-6 is a valid CAS Registry Number.
75883-48-6Relevant academic research and scientific papers
Synthesis and Antiarrhythmic Activity of New Benzofuran Derivatives
Bourgery, Guy,Dostert, Philippe,Lacour, Alain,Langlois, Michel,Pourrias, Bernard,Tisne-Versailles, Jacky
, p. 159 - 167 (2007/10/02)
Various 5-aminobenzofuran derivatives were prepared from khellin and screened intravenously in the dog for their potential antiarrhythmic activity against ouabain-induced ventricular arrhythmia and in the Harris test.From systematic structural variations it was found that two methoxy groups in positions 4 and 7 on the benzofuran ring, a tertiary aminoethoxy side chain in position 6, and a N-methylurea group in position 5 led to the most active compounds.These were then tested orally in the Harris test in the dog.The two long-acting derivativesN--N'-methylurea (8j) and N--N'-methylurea (8m) showed advantages when compared to quinidine and diisopyramide and have been selected for further studies.
