2226-08-6 Usage
Bicyclic structure
The compound has a bicyclic carbon ring system.
Derivative of adamantane
It is derived from the chemical compound adamantane.
Organic synthesis
It is commonly used in organic synthesis.
Chiral building block
It is used as a chiral building block in the production of pharmaceuticals.
Unique structure and stereochemistry
Its structure and stereochemistry make it a valuable intermediate in the synthesis of various compounds.
Resolving agent for racemic mixtures
It is used as a resolving agent to separate racemic mixtures into their individual enantiomers.
Hydroxyl group
The molecule has a hydroxyl group attached to the bicyclic carbon ring.
Versatile platform for chemical modifications
The presence of the hydroxyl group makes it a versatile platform for further chemical modifications and reactions.
Potential applications in new materials
It has potential applications in the development of new materials.
Chiral auxiliary in asymmetric synthesis
It is used as a chiral auxiliary in asymmetric synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 2226-08-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,2 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2226-08:
(6*2)+(5*2)+(4*2)+(3*6)+(2*0)+(1*8)=56
56 % 10 = 6
So 2226-08-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H20O/c1-11(2)9-4-3-8(7-9)10(11)5-6-12/h8-10,12H,3-7H2,1-2H3
2226-08-6Relevant articles and documents
Synthesis in the Isocamphane Series, XXIV. The Synthesis of endo-Configurated Isocamphane Derivatives
Vitek, Renate,Buchbauer, Gerhard
, p. 801 - 820 (2007/10/02)
The syntheses of 46 endo-configurated isocamphane derivatives starting from camphenilanic acid (1) are described.The endo-configuration of the new compounds at position 2 of the bicyclus was retained throughout as has been established by 1H-NMR spectroscopy. - Keywords: Camphenilanic acid; Bicycloheptane; Aldol reaction; Grignard reaction; Enones
