83053-63-8 Usage
Explanation
Different sources of media describe the Explanation of 83053-63-8 differently. You can refer to the following data:
1. The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 19 carbon (C) atoms, 20 hydrogen (H) atoms, and 1 oxygen (O) atom.
2. 11-hydroxygona-1(10),2,4,6,8(14),9(11),12-heptaen-17-one belongs to the steroid family, which is a group of organic compounds with a specific carbon skeleton structure.
3. The compound is derived from gona-1,3,5(10)-triene, a naturally occurring steroid, which means it has a similar structure but with some modifications.
4. As a ketone, the compound contains a carbonyl group (C=O) bonded to two carbon atoms, which is a common functional group in organic chemistry.
5. 11-hydroxygona-1(10),2,4,6,8(14),9(11),12-heptaen-17-one may have pharmacological properties, meaning it could have an effect on biological systems and be of interest in medical research.
6. The exact properties of this compound are not yet fully understood, indicating that more research is needed to determine its potential uses and effects.
7. Due to the limited understanding of its properties, further studies may be necessary to explore the compound's potential applications and effects on biological systems.
Steroid Family
Member
Derivative of
Gona-1,3,5(10)-triene
Type of Compound
Ketone
Pharmacological Properties
Potential
Biological and Chemical Properties
Not fully understood
Further Studies
Required
Check Digit Verification of cas no
The CAS Registry Mumber 83053-63-8 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 83053-63:
(7*8)+(6*3)+(5*0)+(4*5)+(3*3)+(2*6)+(1*3)=118
118 % 10 = 8
So 83053-63-8 is a valid CAS Registry Number.
83053-63-8Relevant articles and documents
Potentially Carcinogenic Cyclopentaphenanthrenes. Part 12. Synthesis of Metabolites of the Carcinogen 16,17-Dihydro-11-methoxy-15H-cyclopentaphenanthrene
Coombs, Maurice M,Boyd, Gary W.
, p. 2901 - 2911 (2007/10/03)
Starting with 15,16-dihydro-11-methoxycyclopentaphenanthren-17-one, the isomeric 15- and 16-keto analogues have been synthesized along with all three isomeric secondary alcohols, the 16,17-trans-diol, and a number of other derivatives. Several of these compounds occur as metabolites of the title methoxy hydrocarbon. 16-Bromo-11-methoxycyclopentaphenanthren-17-one resists dehydrobromination to the corresponding 15(16)-en-17-one, a reaction which proceeds readily with the 16-bromides of the unsubstituted- and 11-methyl-17-ketones.
