21003-06-5 Usage
Chemical class
Dicyclo compounds and secoestran hormones
17-hydroxy-1,5:1,9-dicyclo-9,10-secoestran-4-one belongs to a specific class of chemical compounds, which may share similar properties and structures.
Derivative of estradiol
Yes
It is a derivative of the hormone estradiol, which is a primary female sex hormone.
Role in female reproductive system
Regulation
The compound plays a critical role in the regulation of the female reproductive system, likely due to its structural similarity to estradiol.
Presence of hydroxy group
Yes
The compound contains a hydroxy group, which may contribute to its unique properties and potential biological activities.
Presence of dicyclo structure
Yes
The dicyclo structure in the compound is another factor that gives it unique properties and potential biological activities.
Potential applications
Pharmaceutical research and development
The compound may have applications in pharmaceutical research and development, particularly in the study and modulation of hormonal pathways and related diseases.
Further research needed
Yes
More research is required to fully understand the potential uses and effects of 17-hydroxy-1,5
1,9-dicyclo-9,10-secoestran-4-one.
Biological activities
Unknown (requires further research)
The specific biological activities of 17-hydroxy-1,5:1,9-dicyclo-9,10-secoestran-4-one are not detailed in the provided material, but they are likely related to its structural features and its role in hormonal regulation.
The compound's structure is characterized by these specific features, which contribute to its unique properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 21003-06-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,0,0 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 21003-06:
(7*2)+(6*1)+(5*0)+(4*0)+(3*3)+(2*0)+(1*6)=35
35 % 10 = 5
So 21003-06-5 is a valid CAS Registry Number.
21003-06-5Relevant academic research and scientific papers
PHOTOLYSIS OF 3-OXO-Δ5(10)-STEROIDS IN ALCOHOLIC SOLVENTS AND IN THE SOLID PHASE
Williams, John R.,Abdel-Magid, Ahmed
, p. 1675 - 1678 (2007/10/02)
Irradiation of the β,γ-unsaturated ketone 1a in alcoholic solvents afforded the 1,2 and 1,3-acyl shift products 2a and 3 respectively.The cyclobutanone 3 underwent further photochemistry incorporating a molecule of solvent and affording the ring expanded cyclic acetal 6.Solid phase irradiation of 1a yielded 2a and 3 but 1b was photostable.
