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24268-39-1

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24268-39-1 Usage

Description

[1S,(-)]-1,2,3,4,4aα,5,6,8aα-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene is a sesquiterpene with an octahydronaphthalene structure. It is characterized by the presence of isopropyl, methylene, and methyl groups at positions 1, 4, and 7, respectively, and has the 1S,4aS,8aR-diastereoisomer configuration.

Uses

Used in Pharmaceutical Industry:
[1S,(-)]-1,2,3,4,4aα,5,6,8aα-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene is used as a pharmaceutical compound for its potential therapeutic applications. The compound's unique structure and functional groups may allow it to interact with various biological targets, making it a candidate for the development of new drugs.
Used in Chemical Synthesis:
In the chemical industry, [1S,(-)]-1,2,3,4,4aα,5,6,8aα-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene can be used as a starting material or intermediate in the synthesis of other complex organic compounds. Its specific functional groups and stereochemistry make it a valuable building block for creating a variety of molecules with different applications.
Used in Fragrance Industry:
Due to its unique chemical structure, [1S,(-)]-1,2,3,4,4aα,5,6,8aα-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene may also be used in the fragrance industry as a component in the creation of various scents. Its ability to contribute to the overall aroma profile of a fragrance can make it a valuable addition to the industry's chemical library.
Used in Research and Development:
In the field of research and development, [1S,(-)]-1,2,3,4,4aα,5,6,8aα-Octahydro-7-methyl-4-methylene-1-isopropylnaphthalene can serve as a model compound for studying the properties and reactivity of sesquiterpenes. This can help researchers gain a better understanding of the underlying chemistry and potentially lead to the discovery of new applications and uses for this class of compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 24268-39-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,2,6 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 24268-39:
(7*2)+(6*4)+(5*2)+(4*6)+(3*8)+(2*3)+(1*9)=111
111 % 10 = 1
So 24268-39-1 is a valid CAS Registry Number.

24268-39-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,4a,5,6,8a-octahydro-7-methyl-4-methylene-1-(1-methylethyl)-(1α,4aα,8aα)-naphthalene

1.2 Other means of identification

Product number -
Other names γ-muurolene

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:24268-39-1 SDS

24268-39-1Relevant articles and documents

A multiproduct terpene synthase from medicago truncatula generates cadalane sesquiterpenes via two different mechanisms

Garms, Stefan,Koellner, Tobias G.,Boland, Wilhelm

supporting information; experimental part, p. 5590 - 5600 (2010/11/20)

Terpene synthases are responsible for a large diversity of terpene carbon skeletons found in nature. The multiproduct sesquiterpene synthase MtTPS5 isolated from Medicago truncatula produces 27 products from farnesyl diphosphate (1, FDP). In this paper, we report the reaction steps involved in the formation of these products using incubation experiments with deuterium-containing substrates; we determined the absolute configuration of individual products to establish the stereochemical course of the reaction cascade and the initial conformation of the cycling substrate. Additional labeling experiments conducted with deuterium oxide showed that cadalane sesquiterpenes are mainly produced via the protonation of the neutral intermediate germacrene D (5). These findings provide an alternative route to the general accepted pathway via nerolidyl diphosphate (2, NDP) en route to sesquiterpenes with a cadalane skeleton. Mutational analysis of the enzyme demonstrated that a tyrosine residue is important for the protonation process.

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