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1-(4-methylphenyl)non-1-en-3-one, with the molecular formula C16H22O, is an organic compound classified under the ketone family. It features a carbonyl group (C=O) attached to two carbon atoms, and its structure is distinguished by a non-1-en-3-one functional group, which includes a 1-ene double bond and a ketone group. Additionally, it contains a 4-methylphenyl group, a benzene ring with a methyl substituent.

74975-52-3

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74975-52-3 Usage

Uses

Used in Organic Synthesis:
1-(4-methylphenyl)non-1-en-3-one is utilized as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure allows it to serve as a building block in the creation of complex organic molecules, contributing to the development of new materials and pharmaceuticals.
Used in the Food Industry:
In the food industry, 1-(4-methylphenyl)non-1-en-3-one is employed as a flavoring agent. Its distinct chemical structure imparts specific aromatic properties that can enhance the taste and aroma of various food products, making it a valuable addition to the flavorist's toolbox.

Check Digit Verification of cas no

The CAS Registry Mumber 74975-52-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74975-52:
(7*7)+(6*4)+(5*9)+(4*7)+(3*5)+(2*5)+(1*2)=173
173 % 10 = 3
So 74975-52-3 is a valid CAS Registry Number.

74975-52-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (E)-1-(4-methylphenyl)non-1-en-3-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:74975-52-3 SDS

74975-52-3Relevant academic research and scientific papers

Heteropoly compound catalyzed synthesis of both z- and e-α,β- unsaturated carbonyl compounds

Egi, Masahiro,Umemura, Megumi,Kawai, Takuya,Akai, Shuji

supporting information; experimental part, p. 12197 - 12200 (2012/01/19)

An EZ switch: The cationic species of the heteropoly compounds has a critical impact on the Z/E selectivity of the Meyer-Schuster rearrangement of propargyl alcohols (see scheme). The isolation of the thermodynamically unfavorable Z-α,β-unsaturated carbonyl compounds is notable. The high Z selectivities were obtained at a reaction temperature as high as 50°C.

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