55220-87-6 Usage
Structure
A derivative of naphthalenone with a hexahydro structure, an ethynyl group at the 7th position, and methyl groups at the 1st and 4a positions
Class
Cytotoxic naphthoquinones
Properties
Saturated ketone
Biological activities
Anticancer, antifungal, and antimicrobial properties
Pharmaceutical applications
Potential use in the development of drugs for cancer, fungal infections, and microbial infections
Importance in medicinal chemistry
Unique structure and functional groups make it an interesting target for further research and development in the field.
Check Digit Verification of cas no
The CAS Registry Mumber 55220-87-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,2,2 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55220-87:
(7*5)+(6*5)+(5*2)+(4*2)+(3*0)+(2*8)+(1*7)=106
106 % 10 = 6
So 55220-87-6 is a valid CAS Registry Number.
55220-87-6Relevant articles and documents
Synthesis of Sesquiterpenes, Occidentalol, Chamaecynone and Related Compounds Characterised by a cis-Eudesmane Structure
Mizuno, Yukio,Mori, Reiko
, p. 2849 - 2854 (2007/10/02)
In continuation of our synthetic work for constructing the cis-decalin skeleton by a double Michael annulation using 3-methyl-4-methylenecyclohex-2-enone and its congeners with dimethyl 3-oxoglutarate, the sesquiterpenes, occidentalol, chamaecynone, and related compounds have been synthesised in a stereoselective manner.
Total synthesis of dl chamaecynone, a termiticidal norsesquiterpene
Harayama,Cho,Inubushi
, p. 3273 - 3276 (2007/10/10)
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