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13567-42-5

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13567-42-5 Usage

Description

[3R-(3alpha,3abeta,5alpha,6beta,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5-ol is a complex organic compound that belongs to the class of sesquiterpene alcohols. It is characterized by a unique molecular structure with multiple fused rings and various stereocenters, including methyl groups and a cyclohexane ring system. [3R-(3alpha,3abeta,5alpha,6beta,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5-ol is derived from natural sources such as plants and essential oils.

Uses

Used in Pharmaceutical Industry:
[3R-(3alpha,3abeta,5alpha,6beta,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5-ol is used as a potential pharmaceutical compound for its possible biological activities. [3R-(3alpha,3abeta,5alpha,6beta,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5-ol's complex structure and natural origin suggest that it may have therapeutic properties that could be harnessed for the development of new drugs.
Used in Fragrance Industry:
In the fragrance industry, [3R-(3alpha,3abeta,5alpha,6beta,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5-ol is used as a component in the creation of various scents. Its unique structure and natural origin contribute to the development of novel and complex fragrances.
Used in Flavor Industry:
Similarly, in the flavor industry, [3R-(3alpha,3abeta,5alpha,6beta,7beta,8aalpha)]-octahydro-3,6,8,8-tetramethyl-1H-3a,7-methanoazulen-5-ol is utilized for its potential to enhance or create new flavors in the food and beverage sector. Its intricate molecular structure may provide unique taste profiles that can be beneficial in the development of innovative products.

Check Digit Verification of cas no

The CAS Registry Mumber 13567-42-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,5,6 and 7 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 13567-42:
(7*1)+(6*3)+(5*5)+(4*6)+(3*7)+(2*4)+(1*2)=105
105 % 10 = 5
So 13567-42-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-9-5-6-13-14(3,4)11-7-15(9,13)8-12(16)10(11)2/h9-13,16H,5-8H2,1-4H3

13567-42-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name EINECS 236-973-5

1.2 Other means of identification

Product number -
Other names 2-Isocedranol

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:13567-42-5 SDS

13567-42-5Relevant articles and documents

Bicyclooctenones in Synthesis. A New Synthesis of (+/-)-Cedrene using Sequential Inter- and Intra-molecular Michael Reactions

Horton, Michael,Pattenden, Gerald

, p. 811 - 817 (2007/10/02)

A new synthetic approach to cedrene (1) based on sequential inter- and intra-molecular Michael reactions using the bicyclooctenone (21) as the key intermediate is described.Michael addition of the enolate derived from (21) to 2-nitrobut-2-ene, led to a mixture of diastereoisomers of the nitro ketone (22), which was then converted into the 1,4-dione (23).Treatment of (23) with potassium t-butoxide in t-butyl alcohol resulted in smooth intramolecular Michael reaction leading to a mixture of α- (24a; major) and β-isomers of the tricyclo1,5>undecanedione (24) in a combined yield of 73percent.The undecanedione (24) was then converted into (+/-)-cedrene (1) and the corresponding methyl epimer (31a) via the intermediates (25), (26), (27), and (28).

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