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(6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone is an organic compound characterized by its complex structure, featuring a phenanthridine ring substituted with an ethoxy group and a phenylmethyl ketone group. (6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone is likely to possess pharmacological properties due to the presence of the phenanthridine ring, which is a common motif in many bioactive compounds. The ethoxy group may contribute to the compound's solubility or bioavailability, while the phenylmethyl ketone group could influence its reactivity or biological activity. (6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone's structure hints at potential applications in the fields of pharmacology and biology, although further research and testing are required to confirm its specific properties and uses.

5180-66-5

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5180-66-5 Usage

Uses

Used in Pharmaceutical Industry:
(6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone is used as a potential pharmaceutical compound for its possible pharmacological properties. The presence of the phenanthridine ring, a common feature in many bioactive molecules, suggests that (6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone could have therapeutic applications. Further research is needed to explore its potential as a drug candidate.
Used in Chemical Research:
In the field of chemical research, (6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone can be used as a starting material or a building block for the synthesis of more complex molecules with specific biological activities. Its unique structure, including the phenylmethyl ketone group, may allow for various chemical reactions and modifications, leading to the development of novel compounds with tailored properties.
Used in Drug Delivery Systems:
(6-ethoxyphenanthridin-5(6H)-yl)(phenyl)methanone may also find application in the development of drug delivery systems, particularly if its solubility and bioavailability can be enhanced. The ethoxy group could potentially improve the compound's interaction with biological membranes, facilitating its transport and delivery to target sites within the body. This application would require further investigation into the compound's pharmacokinetics and pharmacodynamics.

Check Digit Verification of cas no

The CAS Registry Mumber 5180-66-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5180-66:
(6*5)+(5*1)+(4*8)+(3*0)+(2*6)+(1*6)=85
85 % 10 = 5
So 5180-66-5 is a valid CAS Registry Number.

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