847577-88-2 Usage
Chemical structure
Contains a dioxane ring, a dimethyl group, an imine functional group, and a benzene ring with a phenylmethoxy substituent.
Functional groups
Dioxane ring, dimethyl group, imine functional group, and phenylmethoxy substituent.
Industrial applications
Used as a building block for the synthesis of other compounds and as a reagent in organic chemistry reactions.
Hazardous properties
Can be hazardous if not used properly, so it is important to handle with care.
Safety precautions
Appropriate safety measures should be taken when handling this chemical, such as wearing protective gear and using proper ventilation.
Molecular weight
Approximately 296.32 g/mol
Physical state
Likely a solid at room temperature, though specific information on its physical state is not provided in the material.
Solubility
The solubility of 1,3-Dioxane-4,6-dione,
2,2-dimethyl-5-[[[4-(phenylmethoxy)phenyl]imino]methyl]- is not provided in the material, but it may be soluble in organic solvents such as ethanol or acetone.
Reactivity
The reactivity of 1,3-Dioxane-4,6-dione,
2,2-dimethyl-5-[[[4-(phenylmethoxy)phenyl]imino]methyl]- is not provided in the material, but it may react with strong acids, strong bases, or other reactive chemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 847577-88-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,5,7 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 847577-88:
(8*8)+(7*4)+(6*7)+(5*5)+(4*7)+(3*7)+(2*8)+(1*8)=232
232 % 10 = 2
So 847577-88-2 is a valid CAS Registry Number.
847577-88-2Relevant academic research and scientific papers
ARYLOXY AND ARYLALKYLENEOXY SUBSTITUTED IMIDAZOQUINOLINES
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Page/Page column 39; 119; 224, (2008/06/13)
Imidazoquinoline compounds with an aryloxy or arylalkyleneoxy or hydroxy substituent at the 6, 7, 8, or 9-position, pharmaceutical compositions containing the compounds, intermediates, and methods of use of these compounds as immunomodulators, for modulating cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases, are disclosed.
ALKOXY SUBSTITUTED IMIDAZOQUINOLINES
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Page/Page column 83, (2008/06/13)
Imidazoquinoline compounds with an alkoxy substituent at the 6, 7, 8, or 9-position, pharmaceutical compositions containing the compounds, intermediates, methods of making, and methods of use of these compounds as immunomodulators, for inducing or inhibit
