25274-27-5

Basic information

• Product Name: (1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one
• Synonyms: (1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one;(1aR,7R,7aR,7bS)-1,1a,4,5,6,7,7a,7b-Octahydro-1,1,7,7a-tetramethyl-2H-cyclopropa[a]naphthalen-2-one;9-Aristolen-8-one;Aristofone;Aristol-9(10)-en-8-one
• CAS NO: 25274-27-5
• Molecular Formula: C15H22O
• Molecular Weight: 218.33458
• Mol File: 25274-27-5.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 308.7±9.0 °C(Predicted)
• Appearance: /
• Density: 1.02±0.1 g/cm3(Predicted)
• CAS DataBase Reference: (1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one(25274-27-5)
• EPA Substance Registry System: (1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one(25274-27-5)

Safety Data

• Hazardous Substances Data: 25274-27-5(Hazardous Substances Data)

Usage

General Description

The chemical compound "(1aR)-1,1aβ,4,5,6,7,7a,7bβ-Octahydro-1,1,7β,7aβ-tetramethyl-2H-cyclopropa[a]naphthalen-2-one" is a type of organic compound with a complex molecular structure. It is a cyclopropane derivative with a cyclopropyl ring fused to a naphthalene ring. The compound contains methyl groups at various positions, giving it a highly symmetrical and stable structure. This chemical may have potential applications in the field of organic synthesis, pharmaceuticals, and materials science due to its unique and intricate molecular architecture. Further research and exploration of its properties and potential uses are warranted to fully understand its capabilities.

Upstream product

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Relevant 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

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.