83053-57-0 Usage
Molecular structure
A complex structure with a 17-carbon backbone and a ketone functional group at the 17th position.
Ethoxy group
An ethoxy group is present at position 11, which contributes to the compound's unique reactivity and physical properties.
Conjugated double bonds
The compound has conjugated double bonds at positions 1, 2, 4, 6, 8, 9, and 12, which also contribute to its unique reactivity and physical properties.
Potential applications
11-ethoxygona-1(10),2,4,6,8(14),9(11),12-heptaen-17-one may have potential applications in organic synthesis, pharmaceuticals, or materials science due to its specific molecular structure and properties.
Further research
More research and studies are needed to fully understand and utilize the potential of this compound.
Please note that the information provided is based on the given material and may not be comprehensive. Further research and analysis may be required to obtain a more detailed understanding of the compound's properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 83053-57-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,5 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83053-57:
(7*8)+(6*3)+(5*0)+(4*5)+(3*3)+(2*5)+(1*7)=120
120 % 10 = 0
So 83053-57-0 is a valid CAS Registry Number.
83053-57-0Relevant articles and documents
CYP1 induction, binding to the hepatic aromatic hydrocarbon receptor and mutagenicity of a series of 11-alkoxy cyclopenta[a]phenanthren-17-ones: a structure activity relationship
Boyd, Gary W.,Coombs, Maurice M.,Ioannides, Costas
, p. 27 - 36 (2007/10/03)
A series of four 11-alkoxy cyclopenta[a]phenathren-17-ones, ranging from the methoxy to the butoxy derivative, has been synthesized in order to investigate the effect of the size of the 11-substituent on the mutagenicity and ability of these compounds to induce hepatic CYP1 activity in rats. The latter was monitored by using as diagnostic probes methoxy and ethoxy-resorufin, and immunologically in Western blots employing anti-CYP1A1 antibodies. All four members of the series induced both CYP1A1 and CYP1A2 activities and apoprotein levels, but the methoxy- and ethoxy-CPP-17-ones were clearly the most potent. Of the four isomers, only 11-methoxy-CPP-17-one displaced (3)H-TCDD from the cytosolic Ah receptor. Similarly only 11-methoxy-CPP-17-one elicited a positive mutagenic response in the Ames test in the presence of an Aroclor 1254-induced activation system. The relevance of these findings to the carcinogenicity of these compounds in the mouse skin painting model is discussed.
