2051-30-1 Usage
Description
2,6-DIMETHYLOCTANE, also known as Myrcane, is a branched alkane hydrocarbon with the molecular formula C10H22. It is a colorless liquid at room temperature and is commonly used as a synthetic intermediate in the chemical industry due to its unique structural properties.
Uses
Used in Chemical Synthesis:
2,6-DIMETHYLOCTANE is used as a synthetic intermediate for the production of various alcohols via C-H hydroxylation of alicyclic and aliphatic compounds. Its unique branching pattern allows for selective functionalization, making it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,6-DIMETHYLOCTANE can be used as a starting material for the synthesis of various drug molecules. Its ability to undergo selective functionalization makes it a versatile component in the development of new therapeutic agents.
Used in Petrochemical Industry:
2,6-DIMETHYLOCTANE can also be utilized in the petrochemical industry as a component in the production of fuels and lubricants. Its high branching and low pour point make it a desirable additive for improving the performance characteristics of these products.
Used in Flavor and Fragrance Industry:
Due to its unique odor profile, 2,6-DIMETHYLOCTANE can be employed in the flavor and fragrance industry as a component in the creation of various scents and flavors. Its ability to mimic natural aromas makes it a valuable asset in the development of new fragrances and flavor compounds.
Used in Research and Development:
In academic and industrial research settings, 2,6-DIMETHYLOCTANE serves as a model compound for studying various chemical reactions and processes. Its well-defined structure and reactivity make it an ideal candidate for investigating reaction mechanisms and developing new synthetic methodologies.
Check Digit Verification of cas no
The CAS Registry Mumber 2051-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,5 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2051-30:
(6*2)+(5*0)+(4*5)+(3*1)+(2*3)+(1*0)=41
41 % 10 = 1
So 2051-30-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H22/c1-5-10(4)8-6-7-9(2)3/h9-10H,5-8H2,1-4H3
2051-30-1Relevant articles and documents
The formation features of C10–C20 regular petroleum isoprenanes
Gordadze,Giruts,Poshibaeva,Koshelev
, p. 672 - 676 (2016/10/04)
To model the formation processes of C10–C20 petroleum isoprenanes, thermolysis of regular and irregular C20–C40 isoprenanes (phytane, crocetane, squalane, and lycopane) and the suggested precursors of regular pe
High-performance ring-opening catalysts based on iridium-containing zeolite Beta in the hydroconversion of decalin
Santi, Dominic,Holl, Tobias,Calemma, Vincenzo,Weitkamp, Jens
, p. 46 - 57 (2013/06/04)
Decalin was converted in a flow-type reactor under a hydrogen pressure of 5.2 MPa on Ir/H,A-Beta zeolite catalysts, where A stands for an alkali metal cation. In one series of catalysts, the Ir content was 3 wt.%, and the nature of A was varied from lithi
Two-stage Reduction of Carbon Dioxide by Hydrogen in a Discharge and in the Presence of a Cobalt-Zirconium Catalyst Deposited on Kieselguhr
Eremin, E. N.,Rubstsova, E. A.,Ivanter, V. I.,Belova, V. M.
, p. 1722 - 1724 (2007/10/02)
The reduction of carbon dioxide by hydrogen has been investigated in a circulation system at a pressure of 1066 GPa, for discharge parameters of 1.9 kV and 150 mA, and at a temperature of 190 to 195 deg C in the catalytic reactor.The overall rate of the reaction was determined by the rate of its catalytic stage; for a contact time between the gas and the catalyst shorter than 3 s, the reaction is displaced towards the formation of paraffinic hydrocarbons.The qualitative and quantitative compositions of the liquid phase depended on its condensation conditions.At positive condensation temperatures, a condensate with relatively heavy components was obtained, up to 60-80percent of which consisted of C9H20-C12 H26 hydrocarbons.Their predominance in the condensate can be explained by secondary reactions on the catalyst involving relatively light saturated hydrocarbons.
