7145-20-2 Usage
Uses
Used in Organic Synthesis:
2,3-DIMETHYL-2-HEXENE is used as a reagent in organic synthesis for its ability to participate in various chemical reactions, contributing to the formation of complex organic compounds.
Used in Perfume Production:
In the fragrance industry, 2,3-DIMETHYL-2-HEXENE is utilized as a precursor for creating perfumes, capitalizing on its sweet odor to enhance the scent profiles of various fragrances.
Used in Flavoring Agents:
2,3-DIMETHYL-2-HEXENE is also employed in the production of flavoring agents, where its distinctive smell can be incorporated into food products or beverages to improve taste and aroma.
Used in Industrial Applications:
2,3-DIMETHYL-2-HEXENE finds use in a variety of industrial applications, serving as a building block for the development of different organic compounds that are essential across multiple sectors.
Used in Organic Chemistry Research:
Furthermore, 2,3-DIMETHYL-2-HEXENE has been studied for its potential use in organic chemistry reactions, providing insights into the behavior of alkenes and their role in the synthesis of other organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 7145-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 5 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7145-20:
(6*7)+(5*1)+(4*4)+(3*5)+(2*2)+(1*0)=82
82 % 10 = 2
So 7145-20-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H16/c1-5-6-8(4)7(2)3/h5-6H2,1-4H3
7145-20-2Relevant academic research and scientific papers
METHOD FOR PRODUCING O-XYLENE
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Page/Page column 13, (2010/01/31)
A process for preparing o-xylene comprises the steps of a) dimerizing 2-butenes to 3,4- and/or 2,3-dimethylhexenes andb) aromatizing the 3,4- and/or 2,3-dimethylhexenes under dehydrogenating conditions to give o-xylene and is suitable for the selective preparation of o-xylene.
Steric and electronic effects on the conformations and singlet oxygen ene regiochemistries of substituted tetramethylethylenes. The origin of the geminal effect
Clennan, Edward L.,Chen, Xiangning,Koola, Jaya J.
, p. 5193 - 5199 (2007/10/02)
The reactions of singlet oxygen with 22 allylically substituted tetramethylethylenes have been studied. Steric and electronic effects on the regiochemistries of the ene reactions have been discovered. Large groups and electron-rich groups increase geminal hydrogen abstraction. Molecular mechanics calculations have been conducted and reveal that the site of hydrogen abstraction is correctly predicted by the rotational barriers of the methyl groups.
Lactone production
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, (2008/06/13)
Gamma-butyrolactones are prepared by the reaction of carbon monoxide with a 3-alkene-1-ol in the presence of a platinum group metal compound.
