16325-63-6 Usage
Description
2,4,4-Trimethyl-1-pentanol, also known as 2,2,4-trimethylpentane metabolite, is a clear colorless liquid that serves as the principal metabolite of 2,2,4-trimethylpentane. It has been studied for its phase equilibria in supercritical carbon dioxide, indicating its potential applications in various industries.
Uses
Used in Chemical Industry:
2,4,4-Trimethyl-1-pentanol is used as a chemical intermediate for the synthesis of various compounds and materials. Its unique chemical structure allows it to be a valuable building block in the creation of different products, such as fragrances, flavors, and specialty chemicals.
Used in Pharmaceutical Industry:
As a metabolite, 2,4,4-trimethyl-1-pentanol may have potential applications in the pharmaceutical industry, particularly in drug development and formulation. Its interaction with supercritical carbon dioxide could be exploited for enhanced drug delivery systems and improved bioavailability of certain medications.
Used in Research and Development:
2,4,4-Trimethyl-1-pentanol is used as a subject of study in research and development, particularly in the fields of chemistry, material science, and engineering. Its phase equilibria properties in supercritical carbon dioxide make it an interesting candidate for further investigation into its potential applications and uses in various industries.
Used in Environmental Applications:
Due to its compatibility with supercritical carbon dioxide, 2,4,4-trimethyl-1-pentanol may find use in environmental applications, such as green chemistry processes and the development of more sustainable technologies. Its properties could be harnessed to improve the efficiency of certain processes and reduce the environmental impact of industrial operations.
Check Digit Verification of cas no
The CAS Registry Mumber 16325-63-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,3,2 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16325-63:
(7*1)+(6*6)+(5*3)+(4*2)+(3*5)+(2*6)+(1*3)=96
96 % 10 = 6
So 16325-63-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H18O/c1-7(6-9)5-8(2,3)4/h7,9H,5-6H2,1-4H3/t7-/m0/s1
16325-63-6Relevant articles and documents
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Brown,H.C. et al.
, p. 1443 - 1447 (1966)
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Generation of iminyl copper species from α-azido carbonyl compounds and their catalytic C-C bond cleavage under an oxygen atmosphere
Chiba, Shunsuke,Zhang, Line,Ang, Gim Yean,Hui, Benjamin Wei-Qiang
supporting information; experimental part, p. 2052 - 2055 (2010/07/04)
Figure presented A copper-catalyzed reaction of α-azidocarbonyl compounds under an oxygen atmosphere is reported where nitriles are formed via C-C bond cleavage of a transient iminyl copper intermediate. The transformation is carried out by a sequence of denitrogenative formation of iminyl copper species from α-azidocarbonyl compounds and their C-C bond cleavage, where molecular oxygen (1 atm) is a prerequisite to achieve the catalytic process and one of the oxygen atoms of O2 was found to be incorporated into the β-carbon fragment as a carboxylic acid.
Hydrocarbon Oxidations with Hydrogen Peroxide Catalyzed by a Soluble Polymer-Bound Manganese(IV) Complex with 1,4,7-Triazacyclononane
Nizova, Galina V.,Bolm, Carsten,Ceccarelli, Simona,Pavan, Chiara,Shul'pin, Georgiy B.
, p. 899 - 905 (2007/10/03)
Soluble manganese(IV) complexes with polymer-bound 1,4,7-triazacyclononanes as ligands (compound 2) catalyze the oxidation of alkanes by hydrogen peroxide in acetonitrile at room and lower temperatures. The corresponding alkyl hydroperoxides are the main products. The presence of a relatively small amount of acetic acid is obligatory for this reaction. The oxidation of alkanes and olefins exhibits some features (kinetic isotope effect, bond selectivities) that distinguish this system from an analogous one based on the dinuclear Mn(IV) complex 1.
