27335-33-7

Basic information

• Product Name: 1R-trans-methyl caronaldehydate
• Synonyms: 1R-trans-methyl caronaldehydate
• CAS NO: 27335-33-7
• Molecular Formula: C₈H₁₂O₃
• Molecular Weight: 156.18
• Mol File: 27335-33-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 186.8±33.0 °C(Predicted)
• Appearance: /
• Density: 1.149±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1R-trans-methyl caronaldehydate(CAS DataBase Reference)
• NIST Chemistry Reference: 1R-trans-methyl caronaldehydate(27335-33-7)
• EPA Substance Registry System: 1R-trans-methyl caronaldehydate(27335-33-7)

Safety Data

• Hazardous Substances Data: 27335-33-7(Hazardous Substances Data)

Usage

Derivative of caronaldehyde

It is a modified version of caronaldehyde, a bicyclic monoterpene ketone found in various essential oils.

Unique structure

The compound has a special structure containing a ring of ten carbon atoms with two oxygen atoms attached.

Usage in fragrance and flavor industry

1R-trans-methyl caronaldehydate is commonly used in perfumes, cosmetics, and food flavorings due to its pleasant, sweet, floral, and fruity aroma.

Potential antimicrobial properties

Studies have been conducted on this chemical compound to explore its possible ability to inhibit the growth of microorganisms, which could be beneficial in various applications.

Potential anti-inflammatory properties

1R-trans-methyl caronaldehydate has also been studied for its possible ability to reduce inflammation, making it a valuable ingredient in products targeting inflammation-related issues.

Upstream product

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• 27335-35-9 (+/-)-(1R,2S)-2-(methoxycarbonyl)-3,3-dimethyl-1-cyclopropanecarboxylic acid 
• 78984-87-9 methyl 4,5-epoxy-3,3-dimethylpentanoate 
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• 713-27-9 (+/-)-2,2-Dimethyl-cis-3-(1-oxo-2-hydroxy-2-methyl-propyl)-cyclopropan-1-carbonsaeure 
• 702-50-1 2,2,5,5-tetramethylcyclohexa-1,3-dione 

Downstream Products

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Relevant articles and documents

Novel synthesis of (d,l) trans-chrysanthemic acid involving a β-diketone fragmentation

Methyl (d,l) trans-chrysanthemate as well as its cis-diastereoisomer have been prepared from dimethyl dimedone, one of their isomers, in a few steps and with complete control of the relative stereochemistry.

ALLYLIC STEREOCENTRE DIRECTED CYCLOPROPANATION. A NEW HIGHLY ENANTIOSELECTIVE SYNTHESIS OF HEMICARONIC ALDEHYDE

isopropyledenetriphenylphosphorane reacts with oxazolidine 4 with excellent ?-face selectivity.The title compound is obtained in high optical purity after removal of the chiral auxiliary.

A SYNTHESIS OF TRANS- AND CIS-CARONALDEHYDES

A preparation of trans- and cis-caronaldehyde derivatives is described by employing iodolactonization reaction as a key step.Investigation is also carried out to establish an asymmetric synthesis by employing the same methodology which allows diastereoselective formation of optically active intermediates in both enantiomeric forms from a single precursor though the degree of asymmetric induction is found to be less satisfactory.