21922-58-7 Usage
Uses
Used in Flavor and Fragrance Industry:
1,5-Dimethylbicyclo[3.2.1]octan-8-one is used as a flavoring agent in food and beverages, adding a refreshing and cooling taste to various products. Its pleasant aroma also makes it a popular ingredient in the fragrance industry, where it is incorporated into cosmetics and personal care products to provide a long-lasting and invigorating scent.
Used in Pest Control Products:
Leveraging its insect repellent properties, 1,5-dimethylbicyclo[3.2.1]octan-8-one is used in mothballs and other pest control products. It helps protect fabrics, clothing, and stored items from damage caused by insects, making it an essential component in household and commercial pest management solutions.
Used in Traditional Medicine:
1,5-Dimethylbicyclo[3.2.1]octan-8-one has been utilized in traditional medicine for its anti-inflammatory and analgesic properties. It is believed to help alleviate pain and reduce inflammation, making it a valuable component in various topical ointments, balms, and liniments.
Used in Pharmaceutical Industry:
Due to its cooling and soothing effects, 1,5-dimethylbicyclo[3.2.1]octan-8-one is used in the pharmaceutical industry for the formulation of various medicated products, such as creams, ointments, and inhalants. It is particularly useful in treatments for respiratory conditions, muscle aches, and skin irritations.
Used in Perfumery:
In the perfumery industry, 1,5-dimethylbicyclo[3.2.1]octan-8-one is used as a fixative agent to enhance the longevity and stability of fragrances. Its ability to blend well with other fragrance components makes it an essential ingredient in creating complex and long-lasting scents.
Used in Rubber and Plastics Industry:
1,5-Dimethylbicyclo[3.2.1]octan-8-one is also used in the rubber and plastics industry as a plasticizer and a mold release agent. Its ability to soften and increase the flexibility of plastics and rubbers makes it a valuable additive in the manufacturing process.
Check Digit Verification of cas no
The CAS Registry Mumber 21922-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,9,2 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21922-58:
(7*2)+(6*1)+(5*9)+(4*2)+(3*2)+(2*5)+(1*8)=97
97 % 10 = 7
So 21922-58-7 is a valid CAS Registry Number.
InChI:InChI=1/C10H16O/c1-9-4-3-5-10(2,7-6-9)8(9)11/h3-7H2,1-2H3
21922-58-7Relevant academic research and scientific papers
Productive chloroarene C-Cl bond activation: Palladium/phosphine-catalyzed methods for oxidation of alcohols and hydrodechlorination of chloroarenes
Bei, Xiaohong,Hagemeyer, Alfred,Volpe, Anthony,Saxton, Robert,Turner, Howard,Guram, Anil S.
, p. 8626 - 8633 (2007/10/03)
The palladium/phosphine-catalyzed productive chloroarene C-Cl bond activation provides general, efficient, and functional group friendly methods for the selective oxidation of alcohols and the hydrodechlorination of chloroarenes.
Productive utilization of chlorobenzene: Palladium-catalyzed selective oxidation of alcohols
Guram, Anil S.,Bei, Xiaohong,Turner, Howard W.
, p. 2485 - 2487 (2007/10/03)
(Matrix presented) The palladium/ligand-catalyzed activation of chlorobenzene provides a general, efficient, and functional group friendly method for the selective oxidation of alcohols to carbonyl compounds.
Selective oxidation of alcohols to aldehydes or ketones
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Example 12, (2008/06/13)
Alcohols are oxidized to their corresponding ketone or aldehyde using an aryl chloride oxidant and a metal-ligand complex or metal/ligand composition. This reaction is particularly applicable to aromatic alcohols and cyclic and bicyclic aliphatic alcohols.
TRANSANNULAR ?-CYCLIZATION IN ELECTROPHILIC ADDITIONS TO 1,5-DIMETHYLCYCLOOCTA-1,5-DIENE
Haufe, G.,Wolf, A.,Schulze, K.
, p. 4719 - 4728 (2007/10/02)
Electrophilic additions of Broensted acids to 1,5-dimethylcycloocta-1,5-diene yield syn-8-substituted 1,5-dimethylbicyclooctanes via parallel ?-cyclization and subsequent Wagner-Meerwein type rearrangements.The corresponding anti-isomers are synthesized by nucleophilic substitution in the 8-position.The classical or nonclassical structure of the cationic intermediates is discussed.
Derivatives of 1,5-dimethylbicyclo [3,2,1] octane, the preparation of these compounds and their use as perfume compound
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, (2008/06/13)
Derivative compounds of 1,5-dimethylbicyclo [3,2,1] octane of the general formula STR1 and perfume compositions containing these derivatives, wherein X represents a C=O group, a STR2 group or a STR3 group, in which R1 and R2 are alkyl groups and R3 is an ethylene or trimethylene group which may be substituted with one or more alkyl groups. These derivative compounds may be prepared by oxidation of 1,5-dimethylbicyclo [3,2,1] octan-8-ol or an ester thereof optionally followed by reaction with an alkanol or a 1,2- or 1,3-alkane-diol.
