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695-05-6

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695-05-6 Usage

General Description

TRICYCLO[2.2.1.0(2,6)]HEPTAN-3-ONE, also known as verbenone, is a naturally occurring organic compound with a unique tricyclic structure. It is widely used in the fragrance and flavor industry, adding a woody, floral scent to various products. Verbenone is also utilized in pest management as a pheromone for disrupting the mating behavior of bark beetles. Additionally, it has potential applications in the pharmaceutical industry due to its biological activities, such as antioxidant and antimicrobial properties. Overall, TRICYCLO[2.2.1.0(2,6)]HEPTAN-3-ONE has diverse uses in several industries, making it an important and versatile chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 695-05-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,9 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 695-05:
(5*6)+(4*9)+(3*5)+(2*0)+(1*5)=86
86 % 10 = 6
So 695-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O/c8-7-3-1-4-5(2-3)6(4)7/h3-6H,1-2H2

695-05-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,4,5,6,7-hexahydrotricyclo[2.2.1.0<sup>2,6</sup>]heptan-3-one

1.2 Other means of identification

Product number -
Other names Nortricyclone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:695-05-6 SDS

695-05-6Relevant articles and documents

Protonated cyclopropanes in α-aminoketone deamination

Edwards, Oliver E.,Dixon, John,Elder, John W.,Kolt, Ralph J.,Lesage, Maurice

, p. 2096 - 2115 (2007/10/02)

Deamination of 2-amino-4,4-dideuterio-6,6-dimethylcyclohexanone, 2-exo-amino- and 2-endo-amino-norbornane-3-one, 2-diazo-norbornan-3-one, 2-exo-amino-5,6-exo-dideuterionorbornan-3-one and the corresponding 5,6-endo-dideuterio isomer has been studied.The nature of the products, the deuterium location in them, and the high retention of steric identity in the carbocations are interpreted in terms of ?-bond participation leading to corner- and edge-protonated cyclopropanes as reaction intermediates.Results with other destabilized carbocations are correlated.

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