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15537-55-0

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15537-55-0 Usage

Description

(1alpha,2beta,5alpha)-2-methyl-5-(1-methylethyl)bicyclo[3.1.0]hexan-2-ol, also known as cis-4-Thujanol, is a bicyclic monoterpene alcohol with a unique molecular structure. It is a related compound of (+)-Sabinene, which is a component of juniper berry oil. This organic compound is characterized by its distinct chemical properties and potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
(1alpha,2beta,5alpha)-2-methyl-5-(1-methylethyl)bicyclo[3.1.0]hexan-2-ol is used as a pharmaceutical compound for its potential therapeutic properties. The compound's unique structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetics Industry:
In the cosmetics industry, (1alpha,2beta,5alpha)-2-methyl-5-(1-methylethyl)bicyclo[3.1.0]hexan-2-ol is used as an ingredient in fragrances and perfumes due to its pleasant aroma. Its unique scent profile can contribute to the creation of distinct and memorable fragrances.
Used in Flavor Industry:
(1alpha,2beta,5alpha)-2-methyl-5-(1-methylethyl)bicyclo[3.1.0]hexan-2-ol is also used in the flavor industry as a component in the development of various food and beverage products. Its distinct taste and aroma can enhance the sensory experience of these products.
Used in Antimicrobial Applications:
As a related compound of (+)-Sabinene, which has demonstrated antibacterial and antifungal activity, (1alpha,2beta,5alpha)-2-methyl-5-(1-methylethyl)bicyclo[3.1.0]hexan-2-ol can be used as an antimicrobial agent in various applications, such as in the development of natural preservatives for the food industry or in the formulation of antimicrobial products for the healthcare sector.
Used in Research and Development:
(1alpha,2beta,5alpha)-2-methyl-5-(1-methylethyl)bicyclo[3.1.0]hexan-2-ol serves as a valuable compound for research and development purposes. Its unique structure and properties make it an interesting subject for scientific studies, potentially leading to the discovery of new applications and uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15537-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,3 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15537-55:
(7*1)+(6*5)+(5*5)+(4*3)+(3*7)+(2*5)+(1*5)=110
110 % 10 = 0
So 15537-55-0 is a valid CAS Registry Number.

15537-55-0SDS

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 sabinene hydrate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Food additives -> Flavoring Agents
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:15537-55-0 SDS

15537-55-0Downstream Products

15537-55-0Relevant articles and documents

Cyclopropanation with dibromomethane under grignard and barbier conditions

Brunner, Gerhard,Eberhard, Laura,Oetiker, Juerg,Schroeder, Fridtjof

scheme or table, p. 3708 - 3718 (2010/04/02)

Tertiary Grignard reagents and dibromomethane efficiently cyclopropanate allylic (and certain homoallylic) magnesium and lithium alcoholates at ambient temperature in ether solvents. Lithium (homo)allyl alcoholates are directly cyclopropanated with magnes

Allylic Lithium Oxyanionic Directed and Facilitated Simmons-Smith Cyclopropanation: Stereoselective Synthesis of (±)-cis-Sabinene Hydrate and a Novel Ring Expansion

Cheng, Dai,Kreethadumrongdat, Thanapong,Cohen, Theodore

, p. 2121 - 2123 (2007/10/03)

(matrix presented) The lithium salts of acid-sensitive allyl alcohols, which themselves decompose during Simmons-Smith cyclopropanation, undergo smooth cyclopropanation in the usual stereocontrolled manner. This concept is applied to the most efficient synthesis of (±)-cis-sabinene hydrate and to the cyclopropanation of the anion of a nonisolable allyl alcohol resulting upon workup in a ring-expanded enone. The cyclopropanations are also faster for the lithium salts than for the allyl alcohols themselves.

Tandem lithium-ene cyclization and thiophenoxide expulsion to produce fused vinylcyclopropanes: First observation of allylic lithium oxyanion- induced reactivity and stereoselectivity in intramolecular carbolithiation

Cheng, Dai,Knox, Kevin R.,Cohen, Theodore

, p. 412 - 413 (2007/10/03)

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