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2,6-Octanedione, 8-cyclohexyl-, also known as Cyclohexyl methyl ketone, is a chemical compound with the molecular formula C14H24O2. It is a clear, colorless liquid characterized by a pungent odor. 2,6-Octanedione, 8-cyclohexylis recognized for its use as a flavoring agent and fragrance in various consumer products, as well as serving as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Due to its potential hazards, it requires careful handling to prevent inhalation, ingestion, or skin contact, and proper disposal in accordance with local environmental regulations.

60439-24-9

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60439-24-9 Usage

Uses

Used in Flavor and Fragrance Industry:
2,6-Octanedione, 8-cyclohexylis used as a flavoring agent and fragrance component for its distinctive aromatic properties, enhancing the sensory experience of various consumer products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 2,6-Octanedione, 8-cyclohexylis utilized as an intermediate in the production of medicinal compounds, contributing to the synthesis of active pharmaceutical ingredients.
Used in Organic Compounds Synthesis:
2,6-Octanedione, 8-cyclohexylalso serves as an intermediate in the synthesis of other organic compounds, playing a crucial role in the creation of a wide range of chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 60439-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,3 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60439-24:
(7*6)+(6*0)+(5*4)+(4*3)+(3*9)+(2*2)+(1*4)=109
109 % 10 = 9
So 60439-24-9 is a valid CAS Registry Number.

60439-24-9Relevant academic research and scientific papers

Organocatalytic asymmetric reaction cascade to substituted cyclohexylamines

Zhou, Jian,List, Benjamin

, p. 7498 - 7499 (2007)

We report a new strategy for organocatalytic cascade reactions. Accordingly, enamine catalysis, iminium catalysis, and Bronsted acid catalysis can work in concert in a highly enantioselective organocatalytic cascade sequence toward chiral cis-3-substituted cyclohexylamines. We found that an achiral amine in combination with a catalytic amount of a chiral Bronsted acid can accomplish an aldol addition-dehydration-conjugate reduction-reductive amination to provide potential intermediates of pharmaceutically active compounds in good yields and excellent enantioselectivities. Copyright

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