21915-33-3 Usage
Uses
Used in Organic Chemistry:
9-ethylbicyclo[3.3.1]nonan-9-ol is used as a building block for the synthesis of various bioactive compounds due to its versatile bicyclic structure and functional groups.
Used in Pharmaceutical Research:
9-ethylbicyclo[3.3.1]nonan-9-ol is used as a precursor in the development of medicinal drugs, capitalizing on its ability to be incorporated into complex molecular frameworks.
Used as a Chiral Auxiliary in Asymmetric Synthesis:
9-ethylbicyclo[3.3.1]nonan-9-ol is utilized for its potential as a chiral auxiliary, providing stereochemical control in chemical reactions, which is crucial for the production of enantiomerically pure compounds.
Used in Drug Development:
9-ethylbicyclo[3.3.1]nonan-9-ol is employed in the pharmaceutical industry for its potential pharmacological effects, with ongoing investigations into its applications in drug discovery and therapeutics.
Check Digit Verification of cas no
The CAS Registry Mumber 21915-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,1 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21915-33:
(7*2)+(6*1)+(5*9)+(4*1)+(3*5)+(2*3)+(1*3)=93
93 % 10 = 3
So 21915-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-2-11(12)9-5-3-6-10(11)8-4-7-9/h9-10,12H,2-8H2,1H3
21915-33-3Relevant academic research and scientific papers
Organoboron Compounds, I. - Transformation of Phosphonium Ylides into Phosphane Monoalkylborane Complexes. - Hydroboration Reactions
Bestmann, Hans Juergen,Roeder, Thomas,Suehs, Kurt
, p. 1509 - 1518 (2007/10/02)
Triphenylphosphonium ylides 1 add borane (from 2) with formation of alkylidenetriphenylphosphorane-boranes 3, which rearrange on heating to give the triphenylphosphane-monoalkylborane adducts 6.Compounds 6 can undergo hydroboration reactions.
