6053-89-0

Basic information

• Product Name: 3-cyclopentylpropanal
• Synonyms: 3-cyclopentylpropanal;3-cyclopentylpropanal(SALTDATA: 0.1H2O);3-Cyclopentyl-propionaldehyde;Cyclopentanepropanal;3-Cyclopentylproponal
• CAS NO: 6053-89-0
• Molecular Formula: C₈H₁₄O
• Molecular Weight: 278.7341
• Mol File: 6053-89-0.mol

Chemical Properties

• Boiling Point: 580.3°Cat760mmHg
• Flash Point: 304.8°C
• Appearance: /
• Density: 1.263g/cm³
• Vapor Pressure: 1.85E-13mmHg at 25°C
• Refractive Index: 1.578
• CAS DataBase Reference: 3-cyclopentylpropanal(CAS DataBase Reference)
• NIST Chemistry Reference: 3-cyclopentylpropanal(6053-89-0)
• EPA Substance Registry System: 3-cyclopentylpropanal(6053-89-0)

Safety Data

• Hazardous Substances Data: 6053-89-0(Hazardous Substances Data)

Usage

Uses

Used in Flavor and Fragrance Industry:
3-cyclopentylpropanal is utilized as a flavoring agent in the food and beverage sector, adding a fruity and floral note to various products. Its pleasant aroma makes it a valuable ingredient in enhancing the sensory experience of consumables.
Used in Perfumery:
In the perfume industry, 3-cyclopentylpropanal serves as a key component in the creation of perfumes and fragrances. Its ability to impart a fresh and floral scent makes it an essential element in crafting complex and appealing olfactory compositions.

InChI:InChI=1/C14H15ClN2O2/c1-2-7-16-14(19)10-8-13(18)17(9-10)12-5-3-11(15)4-6-12/h2-6,10H,1,7-9H2,(H,16,19)

Upstream product

• 767-05-5 3-cyclopentyl-1-propanol 
• 142-29-0 cyclopentene 
• 107-02-8 acrolein 

Downstream Products

• 6267-32-9 2-amino-5-cyclopentylpentanoic acid 
• 1371632-30-2 C₂₀H₂₅ClN₂O₃ 
• 1364447-96-0 C₂₂H₃₄N₂O₂ 
• 1364447-66-4 C₂₂H₃₄N₂O₂ 
• 1333222-72-2 ethyl 5-(E)-cyclopentyl-2-[2-(4-phenyl-1H-pyrazol-1-yl)ethyl]pent-2-enoate 

Relevant articles and documents

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NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS

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SULFONAMIDE SUBSTITUTED CHROMAN DERIVATIVES USEFUL AS BETA 3 ADRENORECEPTOR AGONISTS

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Oxidative Cleavage of Methyl Ethers Using the HOF*CH3CN Complex

HOF*CH3CN complex, made easily by bubbling fluorine diluted with nitrogen through aqueous acetonitrile, proved to be a suitable oxidizer for various methyl ethers.Secondary ethers are oxidized to ketones and even to lactones via Baeyer-Villiger type of oxidation.The reaction is ionic, and the reagent's electrophilic oxygen attacks the relatively electron rich C-H bond α to the ether moiety.It was found that the more sterically hindered is the C-H bond in question, the slower the reaction.In cases where this bond is an electron poor one as in benzoin methyl ether (9), no reaction takes place.When labeled H(18)OF*CH3CN is used on a (16)O methyl ether, the resulting ketone possesses only the heavier oxygen isotope.Primary methyl ethers are somewhat slower to react, but they too were oxidized in very good yields to acids via the corresponding aldehydes.