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7391-48-2

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7391-48-2 Usage

Physical State

Clear, colorless liquid.

Odor

Sweet, fruity.

Usage in Industry

Commonly used as a flavoring agent in the food and beverage industry.

Additional Applications

Production of perfumes and fragrances, potential applications in pharmaceutical and cosmetic industries.

Molecular Structure

Cyclic ketone compound.

Commercial and Industrial Value

Versatile and valuable due to its properties.

Check Digit Verification of cas no

The CAS Registry Mumber 7391-48-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7391-48:
(6*7)+(5*3)+(4*9)+(3*1)+(2*4)+(1*8)=112
112 % 10 = 2
So 7391-48-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O2/c1-2-7(9)6-4-3-5-8(6)10/h6H,2-5H2,1H3

7391-48-2SDS

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 2-propanoylcyclopentan-1-one

1.2 Other means of identification

Product number -
Other names 2-propionyl-1-cyclopentanone

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:7391-48-2 SDS

7391-48-2Relevant articles and documents

Synthesis of 2-substituted 1,3-cycloheptanedione via a lewis acid mediated ring expansion reaction

Inomata, Kohei,Endo, Yasuyuki

, p. 997 - 1012 (2014/01/17)

We have established a new route to provide 2-substituted 1,3-cycloheptanediones via a Lewis acid mediated ring expansion reaction of cyclobutanones as the key step. The ring expansion reactions were mediated by a series of Lewis acids. Among the used Lewis acids, ZnI2 was the most practical mediator. This route has succeeded in providing the title compounds even on a multi-gram scale. During the research, the Baeyer-Villiger oxidation of the cyclobutanones to obtain the new bicyclic lactones was also examined. The regioselective oxidation was observed in the case of chlorinated cyclobutanones.

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