3434-79-5 Usage
Chemical compound
It is a chemical compound with a complex molecular structure.
Derivative of estratrien
It is a derivative of estratrien, which is a steroid hormone.
Ether group
It has an ether group attached to the molecule, which gives it unique properties.
Methyl group
It has a methyl group attached to the molecule, which also contributes to its unique properties.
Pharmaceutical and biochemical research
It has potential use in pharmaceutical and biochemical research.
Hormone replacement therapies
It may have potential applications in the development of hormone replacement therapies.
Studying estrogenic compounds
It can be used to study the effects of estrogenic compounds on the human body.
Research interest
It is of interest to researchers and scientists studying the effects of steroid hormones on mammalian physiology and pathology.
Please note that this list is based on the limited information provided in the material and may not be exhaustive. Further research and analysis would be required to fully understand the properties and potential applications of 1,3,5(10)-ESTRATRIEN-3,16-BETA, 17-BETA-TRIOL 3-METHYL ETHER.
Check Digit Verification of cas no
The CAS Registry Mumber 3434-79-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,3 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 3434-79:
(6*3)+(5*4)+(4*3)+(3*4)+(2*7)+(1*9)=85
85 % 10 = 5
So 3434-79-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H26O3/c1-19-8-7-14-13-6-4-12(22-2)9-11(13)3-5-15(14)16(19)10-17(20)18(19)21/h4,6,9,14-18,20-21H,3,5,7-8,10H2,1-2H3/t14-,15-,16+,17+,18+,19+/m1/s1
3434-79-5Relevant academic research and scientific papers
Steroids. LXIX. Cyclisation Reactions of Vicinal Substituted Halogen Carbamoyloxy Steroids
Ponsold, K.,Grosse, P.
, p. 801 - 818 (2007/10/02)
Vicinal halogen urethanes of the cholestane, androstane and estratriene series react by heating under solvolytic conditions to cyclic carbonates of the corresponding cis-diols.By heating under basic conditions the same compounds react preferably to 2-oxazolidinones and if the basic conditions are strong enough by hydrolysis of the oxazolidinones to cis-amine alcohols too.Connections between the nature of the substituent at the urethane group or the steric arrangement of the vicinal groups on one hand and the reactivity to ring closure on the other hand are presented.
