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2-(4-methylpentyl)cyclopentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63807-78-3

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63807-78-3 Usage

Type of compound

Cyclic ketone It is a type of organic compound containing a cyclopentane ring and an alkyl group, with a carbonyl functional group (C=O) attached to the ring.

Structure

Four-carbon alkyl group The compound contains a 4-methylpentyl group, which is a branched alkyl group with a total of four carbon atoms.

Natural occurrence

Found in fruits, flowers, and essential oils 2-(4-methylpentyl)cyclopentanone is present in various natural sources, contributing to their pleasant aroma and taste.

Usage

Flavor and fragrance ingredient Due to its sweet, fruity, and floral notes, 2-(4-methylpentyl)cyclopentanone is commonly used in the flavor and fragrance industry to enhance the aroma and taste of various products.

Applications

Perfumes, cosmetics, and food products The compound is used in the production of perfumes, cosmetics, and food products to add a pleasant aroma and taste to these formulations.

Versatility

Unique chemical structure and properties The specific structure and properties of 2-(4-methylpentyl)cyclopentanone make it a valuable and versatile ingredient in the fragrance and flavor industry.

Check Digit Verification of cas no

The CAS Registry Mumber 63807-78-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,0 and 7 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 63807-78:
(7*6)+(6*3)+(5*8)+(4*0)+(3*7)+(2*7)+(1*8)=143
143 % 10 = 3
So 63807-78-3 is a valid CAS Registry Number.

63807-78-3Downstream Products

63807-78-3Relevant academic research and scientific papers

Catalytic oxidation of alkyl- and cycloalkylcyclanones into lactones

Abbasov,Alimardanov,Suleimanova

, p. 621 - 626 (2007/10/03)

Pilot-plant syntheses of alkyl and cycloalkylcyclanones and their subsequent liquid-phase oxidation into lactones are described. Characteristics of resulting intermediates and target products are reported.

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