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3-methyl-3-(3,4,5-trimethylphenyl)butanoic acid is a complex organic compound with the molecular formula C15H22O2. It is a derivative of butanoic acid, featuring a 3-methyl group and a 3,4,5-trimethylphenyl group attached to the third carbon. This chemical is characterized by its unique structure, which includes a butanoic acid backbone with a methyl group at the third carbon and a phenyl ring substituted with three methyl groups at the third, fourth, and fifth positions. The compound is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its ability to form stable derivatives and its potential to interact with biological targets. Its chemical properties and reactivity make it a subject of interest in organic chemistry and medicinal chemistry research.

5452-54-0

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5452-54-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5452-54-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5452-54:
(6*5)+(5*4)+(4*5)+(3*2)+(2*5)+(1*4)=90
90 % 10 = 0
So 5452-54-0 is a valid CAS Registry Number.

5452-54-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-3-(3,4,5-trimethylphenyl)butanoic acid

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:5452-54-0 SDS

5452-54-0Relevant academic research and scientific papers

Copper-Mediated, Heterogeneous, Enantioselective Intramolecular Buchner Reactions of α-Diazoketones Using Continuous Flow Processing

Crowley, Daniel C.,Lynch, Denis,Maguire, Anita R.

, p. 3794 - 3805 (2018/04/14)

Enantioselective intramolecular Buchner reactions of α-diazoketones can be effected using heterogeneous copper-bis(oxazoline) catalysts in batch or using continuous flow processing in up to 83% ee. The catalyst can be reused up to 7 times without loss of activity. For α-diazoketones 3 and 4, the enantioselection achieved in flow with the immobilized catalyst was comparable with the standard homogeneous catalyzed process.

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