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4-Hydroxy-2-methyl-1-phenylbutan-1-one, also known as 4-hydroxy-2-methyl-1-phenylbutanone or 4-hydroxy-2-methyl-1-phenylbutan-1-one, is an organic compound with the molecular formula C11H14O2. It is a derivative of a ketone, characterized by the presence of a hydroxyl group (-OH) at the 4th carbon position, a methyl group (-CH3) at the 2nd carbon position, and a phenyl group (C6H5) attached to the 1st carbon position. 4-hydroxy-2-methyl-1-phenylbutan-1-one is a colorless to pale yellow liquid with a molecular weight of 178.23 g/mol. It is soluble in organic solvents and has a melting point of 44-46°C. 4-Hydroxy-2-methyl-1-phenylbutan-1-one is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the synthesis of fragrances and flavorings.

7473-82-7

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7473-82-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7473-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7473-82:
(6*7)+(5*4)+(4*7)+(3*3)+(2*8)+(1*2)=117
117 % 10 = 7
So 7473-82-7 is a valid CAS Registry Number.

7473-82-7SDS

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 4-hydroxy-2-methyl-1-phenylbutan-1-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:7473-82-7 SDS

7473-82-7Downstream Products

7473-82-7Relevant academic research and scientific papers

Homohalocyclization: Electrophilic Bromine-Induced Cyclizations of Cyclopropanes

R?sner, Christian,Hennecke, Ulrich

, p. 3226 - 3229 (2015)

An efficient method for the halocyclization of cyclopropanes has been developed. The cyclopropanes undergo a 1,3-addition reaction to form homohalocyclization products compared to conventional alkene halocyclizations. The reaction can be induced by variou

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