90548-80-4 Usage
Molecular structure
1-Propanone, 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-methoxyphenyl)is a complex organic compound consisting of a propanone group attached to a 3-(dimethylamino)-2-[(dimethylamino)methyl]-1-(4-methoxyphenyl) group.
Functional groups
The compound contains several functional groups, including a propanone group, dimethylamino groups, and a methoxyphenyl group.
Potential pharmaceutical or biological activity
The presence of the dimethylamino and methoxyphenyl groups in the compound suggests that it may have pharmaceutical or biological activity, although further research and analysis would be needed to confirm this.
Complexity
The compound has a complex structure, which may make it challenging to study and understand its properties and potential uses.
Research and analysis requirements
Further research and analysis are needed to fully understand the properties and potential uses of this chemical, including its potential pharmaceutical or biological applications.
Check Digit Verification of cas no
The CAS Registry Mumber 90548-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,5,4 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 90548-80:
(7*9)+(6*0)+(5*5)+(4*4)+(3*8)+(2*8)+(1*0)=144
144 % 10 = 4
So 90548-80-4 is a valid CAS Registry Number.
90548-80-4Relevant academic research and scientific papers
Dimmock,Shyam,Hamon,Logan,Raghavan,Harwood,Smith
, p. 887 - 894 (1983)
Series of 3-dimethylamino-1-aryl-1-propanone hydrobromides (IV) and 3-dimethylamino-2-dimethylaminomethyl-1-aryl-1-propanone dihydrobromides (V) were synthesized. Evaluation of these derivatives against P-388 lymphocytic leukemia growth revealed that two compounds show promise as antineoplastic agents. Compounds of the V series were unstable in phosphate buffer (in contrast to series IV), and when the same nuclear substituent was present in both series of compounds, V was ~ 100 times more active than IV in both the stimulation and inhibition of respiration of mitochondria isolated from rat liver cells. Representatives from both series showed that respiration in mitochondria was affected by changing the pH of the aqueous buffer from 7.4 to 6.9 or 6.4 and by reducing the temperature from 37° to 20°. The compounds showed reactivity toward a biomimetic thiol.
