14474-06-7 Usage
Molecular structure
A complex molecular structure with a dodecahydro derivative of cyclopenta [a]phenanthrene and three hydroxyl functional groups at positions 3, 16, and 17.
Chemical classification
A chemical compound belonging to the family of steroids.
Natural sources
Often found in various natural sources, such as plants and animals.
Biological activities
Its biological activities are of interest to researchers due to its potential pharmacological properties.
Research implications
May have implications in various fields, including medicine and biochemistry.
Functional groups
Contains three hydroxyl functional groups at positions 3, 16, and 17.
Positional isomers
The presence of methyl groups at positions 10 and 13.
Hydrocarbon type
A saturated hydrocarbon due to the presence of dodecahydro (12 hydrogen atoms) in its structure.
Melting and boiling points
The melting and boiling points of 10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta [a]phenanthrene-3,16,17-triol are not provided in the material, but they would be influenced by its molecular size, shape, and functional groups.
Applications
The potential applications of 10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta [a]phenanthrene-3,16,17-triol in medicine and biochemistry are mentioned, but specific uses are not provided in the material.
Check Digit Verification of cas no
The CAS Registry Mumber 14474-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,7 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14474-06:
(7*1)+(6*4)+(5*4)+(4*7)+(3*4)+(2*0)+(1*6)=97
97 % 10 = 7
So 14474-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H30O3/c1-18-7-5-12(20)9-11(18)3-4-13-14(18)6-8-19(2)15(13)10-16(21)17(19)22/h3,12-17,20-22H,4-10H2,1-2H3
14474-06-7Relevant academic research and scientific papers
Action de l'anhydride acetique et des chlorures de benzoyle et de p-toluene sulfonyle sur des nitrones derivees de ceto-17 steroides. Conditions conduisant a un rearrangement ou a une fonctionnalisation
Cherest, M.,Lusinchi, X.
, p. 227 - 232 (2007/10/02)
The reaction of the title reagents under anhydrous conditions and in the presence of base leads to steroidal derivatives functionalised at position 16; whereas, in the presence of water, paratoluenesulphonyl chloride gives 17-aza-D-homo lactams by ring expansion, and use of benzoyl chloride promotes a hydrolytic fragmentation.In contrast to earlier studies, the formation of an oxaziridine under aqueous alkaline conditions was not observed in this work.These results, when considered in conjunction with those previously obtained, enable the course of these reactions to be determined as a function of the reaction conditions.
