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25274-27-5

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25274-27-5 Usage

Description

(1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one is a complex organic compound characterized by a cyclopropane ring fused to a naphthalene ring. This cyclopropane derivative features methyl groups at various positions, contributing to its symmetrical and stable molecular structure. Its unique and intricate architecture may offer potential applications in organic synthesis, pharmaceuticals, and materials science, warranting further research and exploration to uncover its full capabilities.

Uses

Used in Organic Synthesis:
(1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one is used as a key intermediate in organic synthesis for the development of novel compounds with specific properties. Its unique molecular structure allows for versatile chemical reactions, facilitating the creation of new organic molecules with potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one is used as a potential drug candidate or a building block for the synthesis of pharmaceutical compounds. Its stable and symmetrical structure may contribute to the development of new drugs with improved efficacy and selectivity.
Used in Materials Science:
(1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one is utilized in materials science for the development of new materials with specific properties. Its molecular structure may contribute to the creation of materials with unique characteristics, such as enhanced stability, improved mechanical properties, or novel optical and electronic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 25274-27-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,7 and 4 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25274-27:
(7*2)+(6*5)+(5*2)+(4*7)+(3*4)+(2*2)+(1*7)=105
105 % 10 = 5
So 25274-27-5 is a valid CAS Registry Number.

25274-27-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (-)-aristolone

1.2 Other means of identification

Product number -
Other names Aristolone

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:25274-27-5 SDS

25274-27-5Downstream Products

25274-27-5Relevant articles and documents

Biotransformation of aristolane- and 2,3-secoaromadendrane-type sesquiterpenoids having a 1,1-dimethylcyclopropane ring by Chlorella fusca var. vacuolata, Mucor species, and Aspergillus niger

Furusawa, Mai,Hashimoto, Toshihiro,Noma, Yoshiaki,Asakawa, Yoshinori

, p. 861 - 868 (2007/10/03)

Biotransformation of the aristolane-type sesquiterpene hydrocarbon (+)-1(10)-aristolene (1) from the crude drug Nardostachys chinensis and of the 2,3-secoaromadendrane-type sesquiterpene lactone plagiochilide (2) from the liverwort Plagiochila fruticosa by three microorganisms, Chlorella fusca var. vacuolata, Mucor species, and Aspergillus niger was investigated. C. fusca var. vacuolata and Mucor sp. introduced oxygen function into the cyclohexane ring of aristolene while A. niger oxidized stereoselectively one methyl of the 1,1-dimethyl group on the cyclopropane ring of aristolanes and 2,3-secoaromadendrane to give C-12 primary alcohol and C-12 carboxylic acid. The possible metabolic pathway of the formation of new metabolites is discussed. The stereostructures of new metabolites were established by a combination of NMR spectroscopy including HMBC and NOESY, X-ray crystallographic analysis, and chemical reaction.

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