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5-(4-methylphenyl)hexan-2-one is an organic compound with the molecular formula C13H18O. It is a colorless to pale yellow liquid with a strong, sweet, and floral odor. This ketone is characterized by a hexane chain with a 4-methylphenyl group attached at the 5th carbon and a ketone group at the 2nd carbon. It is used as a fragrance ingredient in various applications, including perfumes, cosmetics, and household products, due to its pleasant scent. The compound is also known for its potential use in the synthesis of other organic compounds. It is important to note that, like many chemicals, it should be handled with care due to its potential health and environmental impacts.

7511-95-7

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7511-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7511-95-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 1 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7511-95:
(6*7)+(5*5)+(4*1)+(3*1)+(2*9)+(1*5)=97
97 % 10 = 7
So 7511-95-7 is a valid CAS Registry Number.

7511-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(4-methylphenyl)hexan-2-one

1.2 Other means of identification

Product number -
Other names 5-p-tolyl-hexan-2-one

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 -
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More Details:7511-95-7 SDS

7511-95-7Downstream Products

7511-95-7Relevant academic research and scientific papers

A Lewis Base Catalysis Approach for the Photoredox Activation of Boronic Acids and Esters

Lima, Fabio,Sharma, Upendra K.,Grunenberg, Lars,Saha, Debasmita,Johannsen, Sandra,Sedelmeier, Joerg,Van der Eycken, Erik V.,Ley, Steven V.

supporting information, p. 15136 - 15140 (2017/11/20)

We report herein the use of a dual catalytic system comprising a Lewis base catalyst such as quinuclidin-3-ol or 4-dimethylaminopyridine and a photoredox catalyst to generate carbon radicals from either boronic acids or esters. This system enabled a wide range of alkyl boronic esters and aryl or alkyl boronic acids to react with electron-deficient olefins via radical addition to efficiently form C?C coupled products in a redox-neutral fashion. The Lewis base catalyst was shown to form a redox-active complex with either the boronic esters or the trimeric form of the boronic acids (boroxines) in solution.

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