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6948-37-4

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6948-37-4 Usage

Type of compound

Aromatic ketone

Natural occurrence

Found in plants such as ginger

Responsible for

Characteristic spicy aroma and flavor of ginger

Potential medicinal properties

Antioxidant, anti-inflammatory, and anticancer effects

Application

Used as a flavoring agent in food and beverages

Research interest

Prevention and treatment of various diseases, pharmaceutical research

Check Digit Verification of cas no

The CAS Registry Mumber 6948-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6948-37:
(6*6)+(5*9)+(4*4)+(3*8)+(2*3)+(1*7)=134
134 % 10 = 4
So 6948-37-4 is a valid CAS Registry Number.

6948-37-4SDS

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 1-(5-hydroxy-4-methoxy-2-methylphenyl)ethanone

1.2 Other means of identification

Product number -
Other names 5-Hydroxy-4-methoxy-2-methyl-acetophenon

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:6948-37-4 SDS

6948-37-4Downstream Products

6948-37-4Relevant articles and documents

Reexamen de la transposition de Fries des acetate et propionate de creosol

Martin, Robert,Gavard, Jean-Pierre,Delfly, Michel,Demerseman, Pierre,Tromelin, Anne

, p. 659 - 662 (2007/10/02)

The Fries rearrangement of creosol acetate and propionate yields meta acylphenols through meta ketoesters according to an intermolecular process.The acyl group undergoes a migration to the meta position, solely due to the combination of the electronic effects of the other substituents.A similar directing effect occurs in a transacylation reaction between a ketoester of creosol and the creosol itself.The two hitherto unknown propiophenones stemming from isocreosol are synthesized and described.

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