4491-26-3 Usage
Chemical structure
A bicyclic heterocyclic compound containing a quinolizine ring system with a six-membered ring and a nitrogen atom fused to a benzene ring.
Molecular weight
Approximately 211.31 g/mol
Appearance
It is likely to be a solid or crystalline substance, although the exact appearance is not provided in the material.
Potential applications
Organic synthesis and medicinal chemistry
Biological activities
The compound has been studied for its potential biological activities, although specific activities are not mentioned in the material.
Pharmacological properties
The compound has been investigated for its potential pharmacological properties, but the specific properties are not provided in the material.
Solubility
The solubility of 1H-Benzo[c]quinolizine, 2,3,4,4a,5,6-hexahydrois not mentioned in the material, but it may be soluble in organic solvents like ethanol, methanol, or acetone, as is common for many heterocyclic compounds.
Stability
The stability of the compound is not explicitly mentioned in the material, but it is generally expected to be stable under normal laboratory conditions.
Reactivity
The reactivity of 1H-Benzo[c]quinolizine, 2,3,4,4a,5,6-hexahydrois not provided in the material, but it may undergo reactions typical of heterocyclic compounds, such as electrophilic aromatic substitution or nucleophilic addition.
Check Digit Verification of cas no
The CAS Registry Mumber 4491-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,9 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4491-26:
(6*4)+(5*4)+(4*9)+(3*1)+(2*2)+(1*6)=93
93 % 10 = 3
So 4491-26-3 is a valid CAS Registry Number.
4491-26-3Relevant academic research and scientific papers
CATALYSIS IN FLASH VACUUM PYROLYSIS
Hodgetts, I.,Noyce, S. J.,Storr, R. C.
, p. 5435 - 5438 (2007/10/02)
The temperature required for flash pyrolytic elimination of water from o-aminobenzyl alcohols and of carbon dioxide from dihydrobenzoxazinones to give azaxylylenes is considerably lowered by the presence of alumina and silica gel in the hot zone.
GENERATION AND REACTIONS OF AZAXYLYLENES
Bowen, R. D.,Davies, D. E.,Fishwick, C. W. G.,Glasbey, T. O.,Noyce, S. J.,Storr, R. C.
, p. 4501 - 4504 (2007/10/02)
Azaxylenes produced by flash vacuum pyrolysis of 2-aminobenzylalcohols, dihydrobenzoxazinones and dihydrobenzoxazines undergo intramolecular cyclisation, H-shifts or Diels-Alder reactions, depending on their substituents.
