21922-58-7

Basic information

• Product Name: 1,5-dimethylbicyclo[3.2.1]octan-8-one
• Synonyms: 1,5-dimethylbicyclo[3.2.1]octan-8-one;Einecs 244-662-0
• CAS NO: 21922-58-7
• Molecular Formula: C₁₀H₁₆O
• Molecular Weight: 152.23344
• EINECS: 244-662-0
• Mol File: 21922-58-7.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 210.2°Cat760mmHg
• Flash Point: 73.8°C
• Appearance: /
• Density: 1.022g/cm³
• Vapor Pressure: 0.195mmHg at 25°C
• Refractive Index: 1.506
• CAS DataBase Reference: 1,5-dimethylbicyclo[3.2.1]octan-8-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1,5-dimethylbicyclo[3.2.1]octan-8-one(21922-58-7)
• EPA Substance Registry System: 1,5-dimethylbicyclo[3.2.1]octan-8-one(21922-58-7)

Safety Data

• Hazardous Substances Data: 21922-58-7(Hazardous Substances Data)

Usage

General Description

1,5-dimethylbicyclo[3.2.1]octan-8-one, also known as camphor, is a bicyclic organic compound with a camphor-like odor. It is commonly used as a flavoring agent in food and beverages, as well as a fragrance in cosmetics and personal care products. In addition, it has insect repellent properties and is used in mothballs and other pest control products. Camphor is also used in traditional medicine for its anti-inflammatory and analgesic properties. However,

InChI:InChI=1/C10H16O/c1-9-4-3-5-10(2,7-6-9)8(9)11/h3-7H2,1-2H3

Upstream product

• 60329-20-6 1,5-dimethyl-bicyclo-[3,2,1]-octane-8-ol 
• 60329-20-6 1,5-dimethylbicyclo<3.2.1>octan-8-ol 
• 73022-52-3 1,5-dimethyl-1,5-cyclooctadiene 
• 72903-06-1 8-formoxy-1,5-dimethylbicyclo<3.2.1>octane 

Downstream Products

• 112359-33-8 1,5-dimethyl-8-phenyl-exo-bicyclo<3.2.1>octan-8-ol 
• 84681-92-5 1.5-dimethyl-8-ethyl-bicyclo[3.2.1]octane-8-ol 
• 84681-91-4 1,5,8-trimethyl-bicyclo[3.2.1]octane-8-ol 
• 75147-23-8 1,5-dimethyl-8-hydroximino-bicyclo[3.2.1]octane 

Relevant articles and documents

Productive chloroarene C-Cl bond activation: Palladium/phosphine-catalyzed methods for oxidation of alcohols and hydrodechlorination of chloroarenes

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.

Selective oxidation of alcohols to aldehydes or ketones

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.

Derivatives of 1,5-dimethylbicyclo [3,2,1] octane, the preparation of these compounds and their use as perfume compound

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.