10395-51-4 Usage
Uses
Used in Organic Synthesis:
2,2-dimethoxynorbornane is utilized as a reagent in organic synthesis for the formation of various organic molecules. Its stability and inertness contribute to its wide applicability in chemical reactions, making it a valuable asset in the synthesis of complex organic compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2,2-dimethoxynorbornane is studied for its potential applications due to its unique structure and properties. It may serve as a precursor or a building block in the development of new pharmaceutical agents, contributing to the discovery of novel therapeutics.
Used in Materials Science:
2,2-dimethoxynorbornane also finds use in materials science, where its distinctive structural features can be leveraged to create new materials with specific properties. This can include the development of advanced polymers, composites, or other materials with tailored characteristics for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 10395-51-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,9 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 10395-51:
(7*1)+(6*0)+(5*3)+(4*9)+(3*5)+(2*5)+(1*1)=84
84 % 10 = 4
So 10395-51-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-10-9(11-2)6-7-3-4-8(9)5-7/h7-8H,3-6H2,1-2H3
10395-51-4Relevant articles and documents
Thermochemical Studies of Carbonyl Reactions. 4. Enthalpies of Hydrolysis of Norbornyl Ketals
Wiberg, Kenneth B.,Cunningham, Wells C.
, p. 679 - 684 (2007/10/02)
The dimethyl ketals of norbornanone and of eight methyl-substituted norbornanones were prepared, and the enthalpies of hydrolysis were determined.The compounds were chosen to provide a variety of steric interactions between the methyl substituents and the ketal group, much of which would be relieved on going to the ketone.The enthalpies of reaction varied by over 4 kcal/mol.The experimental data were modeled by molecular mechanics (MM2), and although a good correlation was found for the less substituted compounds, the ketal of camphor fell off the slope = 1 correlation line.The free energy changes were determined, and were found not to be well correlated with the enthalpy changes.
