10036-08-5 Usage
Uses
Used in Pharmaceutical Industry:
Exo-Bicyclo[3.3.1]nonan-3-ol is used as a building block for the synthesis of complex molecules in the pharmaceutical industry. Its unique structure and properties make it suitable for the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, exo-Bicyclo[3.3.1]nonan-3-ol is utilized as a starting material for the synthesis of various agrochemicals, including pesticides and herbicides. Its compact and rigid structure allows for the creation of effective and targeted agrochemicals.
Used in Material Development:
Exo-Bicyclo[3.3.1]nonan-3-ol is employed in the development of new materials due to its unique structural properties. Its rigidity and compactness make it a promising candidate for the creation of advanced materials with specific properties and applications.
Used in Organic Synthesis as a Chiral Auxiliary:
In organic synthesis, exo-Bicyclo[3.3.1]nonan-3-ol is used as a chiral auxiliary. Its unique structure allows for the control of stereochemistry during chemical reactions, enabling the synthesis of enantiomerically pure compounds, which are essential in various applications, including pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 10036-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,3 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10036-08:
(7*1)+(6*0)+(5*0)+(4*3)+(3*6)+(2*0)+(1*8)=45
45 % 10 = 5
So 10036-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O/c10-9-5-7-2-1-3-8(4-7)6-9/h7-10H,1-6H2
10036-08-5Relevant academic research and scientific papers
Synthesis and 13C NMR Spectroscopic Investigations of Bridgehead-substituted endo-Bicyclononan-3-ols and Oxaadamantans
Duddeck, Helmut,Wagner, Petra
, p. 1981 - 1988 (2007/10/02)
The syntheses of the title compounds 5 and 7 as well as some other bicyclononane derivatives are reported.The γ-substituent effects on the 13C chemical shifts can readily be interpreted in terms of semiquantitative evaluation of torsional angles in the molecular moieties involved.
Bicyclononanes as Synthetic intermediates. IX.1) Photo-Irradiation of Bicycloalkan-3-one in Cyclohexane: A Selective Photo-Reduction with Predominance of endo-Hydrogenation
Momose, Takefumi,Muraoka, Osamu,Masuda, Kikuo
, p. 3730 - 3733 (2007/10/02)
Predominant formation of exo-alcohols in the photo-irradiation of bicyclononan-3-one and its analogs is described. Keywords --- bicyclononane system; selective photo-reduction; steric hindrance; intermolecular hydrogen abstraction; hydrogen-donor solvent.
