69462-10-8 Usage
Description
2,2,4-Trimethylpentanenitrile, with the CAS number 69462-10-8, is an organic compound that is characterized by its unique chemical structure and properties. It is a versatile molecule with potential applications in various industries due to its distinct chemical properties.
Uses
Used in Bio-Fuels and Bio-Chemicals Production:
2,2,4-Trimethylpentanenitrile is used as a key intermediate for the production of bio-fuels and bio-chemicals. Its unique chemical structure allows it to be a valuable component in the synthesis of these sustainable and environmentally friendly alternatives to traditional fossil fuels and chemicals. The use of 2,2,4-Trimethylpentanenitrile in this application helps to reduce the dependency on non-renewable resources and contributes to a more sustainable future.
Check Digit Verification of cas no
The CAS Registry Mumber 69462-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,6 and 2 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 69462-10:
(7*6)+(6*9)+(5*4)+(4*6)+(3*2)+(2*1)+(1*0)=148
148 % 10 = 8
So 69462-10-8 is a valid CAS Registry Number.
69462-10-8Relevant articles and documents
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Tanner,Rahimi
, p. 1674,1676 (1979)
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An Iodine-Catalyzed Hofmann-L?ffler Reaction
Martínez, Claudio,Mu?iz, Kilian
supporting information, p. 8287 - 8291 (2015/07/07)
Iodine reagents have been identified as economically and ecologically benign alternatives to transition metals, although their application as molecular catalysts in challenging C-H oxidation reactions has remained elusive. An attractive iodine oxidation catalysis is now shown to promote the convenient conversion of carbon-hydrogen bonds into carbon-nitrogen bonds with unprecedented complete selectivity. The reaction proceeds by two interlocked catalytic cycles comprising a radical chain reaction, which is initiated by visible light as energy source. This unorthodox synthetic strategy for the direct oxidative amination of alkyl groups has no biosynthetic precedence and provides an efficient and straightforward access to a general class of saturated nitrogenated heterocycles.