83053-60-5 Usage
Molecular structure
A complex structure with a seven-membered ring and an alkene chain.
Functional group
Contains a ketone group (C=O) and a butoxy group (C4H9O-).
Chemical class
Belongs to the class of organic compounds, specifically ketones.
Stereochemistry
The presence of multiple stereocenters may result in different stereoisomers.
Solubility
Likely to be soluble in organic solvents such as ethanol, methanol, or acetone, due to its nonpolar nature.
Reactivity
May undergo various chemical reactions, such as nucleophilic addition, oxidation, and reduction, due to the presence of the carbonyl group and the alkene chain.
Stability
The stability of the compound may be influenced by factors such as temperature, light exposure, and the presence of other reactive substances.
Synthesis
The synthesis of this compound may be challenging due to its complex structure, requiring multiple steps and careful control of reaction conditions.
Potential applications
Possible uses in organic synthesis, pharmaceuticals, and material science, given its unique structure and properties.
Safety and handling
Due to its complex structure and potential reactivity, appropriate safety measures should be taken when handling this compound, such as using gloves, eye protection, and working in a well-ventilated area.
Environmental impact
The environmental impact of this compound is not well-known, but it may be important to consider factors such as biodegradability, toxicity, and potential for bioaccumulation when assessing its suitability for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 83053-60-5 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, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83053-60:
(7*8)+(6*3)+(5*0)+(4*5)+(3*3)+(2*6)+(1*0)=115
115 % 10 = 5
So 83053-60-5 is a valid CAS Registry Number.
83053-60-5Relevant 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.
