297179-11-4 Usage
Molecular Class
Phenanthrenediol
Explanation
The compound belongs to the phenanthrenediol class of molecules, which are organic compounds containing a specific core structure.
Explanation
The compound consists of 21 carbon atoms, 34 hydrogen atoms, and 2 oxygen atoms.
Explanation
The compound features a long hydrocarbon chain, which may contribute to its potential applications in various fields.
Explanation
The compound has several methyl (CH3) and ethyl (C2H5) groups attached to its hydrocarbon chain, which can influence its chemical properties and reactivity.
Explanation
The compound has a specific spatial arrangement of atoms, with the (4bS, 8aS, 10S) designation indicating the configuration of its chiral centers. This can be important for its biological or chemical activity.
Explanation
Although the exact properties and uses of 2,10-Phenanthrenediol, 4b,5,6,7,8,8a,9,10-octahydro-4b,8,8,10-tetramethyl-1-(1-methylethyl)-, (4bS,8aS,10S)- need further research, it may have potential applications in these fields due to its unique structure and properties.
Explanation
The compound's properties and uses are not yet fully understood, and additional research and experimentation are required to determine its potential applications and effects.
Hydrocarbon Chain
Long
Attached Groups
Methyl and Ethyl
Stereochemistry
(4bS, 8aS, 10S)
Potential Applications
Organic Chemistry, Pharmaceuticals, Materials Science
Further Research
Necessary
Check Digit Verification of cas no
The CAS Registry Mumber 297179-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,7 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 297179-11:
(8*2)+(7*9)+(6*7)+(5*1)+(4*7)+(3*9)+(2*1)+(1*1)=184
184 % 10 = 4
So 297179-11-4 is a valid CAS Registry Number.
297179-11-4Relevant academic research and scientific papers
The synthesis and antibacterial activity of totarol derivatives. Part 3: modification of ring-B
Evans, Gary B.,Furneaux, Richard H.,Gainsford, Graeme J.,Murphy, Michael P.
, p. 1663 - 1675 (2007/10/03)
Ring-B derivatization of totarol (1) afforded the series of compounds 2-22 which were screened in vitro against: β-lactamase-positive and high level gentamycin-resistant Enterococcus faecalis, penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus (MRSA), and multiresistant Klebsiella pneumoniae. Several of the derivatives retained much of the antibacterial activity of totatol against the first three of these organisms (all Gram-positive), but none was more active. The Gram-negative Klebsiella was resistant to all compounds examined. Totarol (1) was shown to uncouple oxidative phosphorylation in isolated mitochondria at 50 μM. Copyright (C) 2000 Elsevier Science Ltd.
