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[1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol, also known as Thujane monoterpenoid, is a chemical compound belonging to the thujane class of monoterpenoids. It features a (1R,4S,5S)-thujane skeleton with a hydroxy group substitution at the C-3 position, and the new asymmetric center at C-3 has an R-configuration. [1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol is characterized by its unique stereochemistry and structural features, which may contribute to its potential applications in various industries.

3284-85-3

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3284-85-3 Usage

Uses

Used in Pharmaceutical Industry:
[1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol is used as a pharmaceutical compound for its potential therapeutic applications. [1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol's unique structure and stereochemistry may allow it to interact with specific biological targets, making it a candidate for the development of new drugs or drug candidates.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, [1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol can be used as a key ingredient in the creation of various scents and flavors. Its unique chemical structure may contribute to the development of novel and distinct fragrances or taste profiles.
Used in Chemical Synthesis:
[1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol can also be utilized as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structural features may facilitate the development of new synthetic routes and methodologies in organic chemistry.
Used in Research and Development:
[1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol can be employed in research and development settings to study its properties, reactivity, and potential applications. Understanding the behavior of [1R(1alpha,3alpha,4alpha,5alpha)]-4-methyl-1-(1-methylethyl)bicyclo[3.1.0]hexan-3-ol in various chemical reactions and biological systems can provide valuable insights into its potential uses and limitations.

Check Digit Verification of cas no

The CAS Registry Mumber 3284-85-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,8 and 4 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3284-85:
(6*3)+(5*2)+(4*8)+(3*4)+(2*8)+(1*5)=93
93 % 10 = 3
So 3284-85-3 is a valid CAS Registry Number.

3284-85-3SDS

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 (+)-thujan-3-ol

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.
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:3284-85-3 SDS

3284-85-3Downstream Products

3284-85-3Relevant academic research and scientific papers

(-) 3 Isothujone, a small nonnitrogenous molecule with antinociceptive activity in mice

Rice,Wilson

, p. 1054 - 1057 (1976)

(-) 3 isothujone and (+) 3 thujone were examined for antinociceptive activity using the hot plate and Nilsen tests. In the hot plate test (-) 3 isothujone (ED50 = 6.5 mg/kg) was found to be codeine like and equipotent with (-) Δ9 tetrahydrocannabinol while the racemic material was essentially half as potent as the levorotatory isomer. (+) 3 Thyjone was inactive in both antinociceptive tests as were several structural analogues of the 3 thujones. As with the THC's less antinociceptive activity was observed in the Nilsen test than in the hot plate assay. Acute toxicities for the 3 thujones were determined and vastly improved synthetic procedures have been developed for two long known but difficultly accessible 3 thujanols.

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