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Cyclohexyl 2,4-dimethylphenyl ketone is an organic compound with the chemical formula C15H20O. It is a ketone derivative, characterized by the presence of a carbonyl group (C=O) bonded to a cyclohexyl group and a 2,4-dimethylphenyl group. CYCLOHEXYL 2,4-DIMETHYLPHENYL KETONE is known for its unique chemical structure, which contributes to its properties and potential applications in various fields, such as pharmaceuticals, fragrances, and chemical research. The compound's molecular weight is 212.32 g/mol, and it is often used as an intermediate in the synthesis of other organic compounds due to its reactivity and stability.

2760-64-7

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2760-64-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2760-64-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2760-64:
(6*2)+(5*7)+(4*6)+(3*0)+(2*6)+(1*4)=87
87 % 10 = 7
So 2760-64-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H20O/c1-11-8-9-14(12(2)10-11)15(16)13-6-4-3-5-7-13/h8-10,13H,3-7H2,1-2H3

2760-64-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclohexyl-(2,4-dimethylphenyl)methanone

1.2 Other means of identification

Product number -
Other names Cyclohexyl(2,4-dimethylphenyl)methanone

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:2760-64-7 SDS

2760-64-7Downstream Products

2760-64-7Relevant academic research and scientific papers

P -Selective (sp2)-C-H functionalization for an acylation/alkylation reaction using organic photoredox catalysis

Pandey, Ganesh,Tiwari, Sandip Kumar,Singh, Bhawana,Vanka, Kumar,Jain, Shailja

, p. 12337 - 12340 (2017/11/20)

p-Selective (sp2)-C-H functionalization of electron rich arenes has been achieved for acylation and alkylation reactions, respectively, with acyl/alkylselenides by organic photoredox catalysis involving an interesting mechanistic pathway.

Friedel-Crafts Acylation of Arenes Catalysed by Bromopentacarbonylrhenium(I)

Kusama, Hiroyuki,Narasaka, Koichi

, p. 2379 - 2384 (2007/10/03)

The intermolecular Friedel-Crafts acylation of aromatic compounds (such as toluene, m-xylene, and anisole) with various acid chlorides proceeds by using a catalytic amount of bromopentacarbonylrhenium(I) to afford aryl ketones.Intramolecular acylation is also catalyzed by the above-mentioned catalyst to give indanone and tetralone derivatives.

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