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(2-Benzylphenyl)(naphthalen-2-yl)methanone, also known as 2-benzyl-2-naphthyl-(phenyl)methanone, is an aromatic ketone with a molecular formula of C28H22O. It is a yellow solid that is sparingly soluble in water. (2-benzylphenyl)(naphthalen-2-yl)methanone is commonly used as a building block in organic synthesis and chemical research.

7424-65-9

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7424-65-9 Usage

Uses

Used in Pharmaceutical Industry:
(2-Benzylphenyl)(naphthalen-2-yl)methanone is used as a chemical intermediate for the development of new drugs due to its unique structure and properties.
Used in Organic Compounds Production:
(2-Benzylphenyl)(naphthalen-2-yl)methanone is used as a key component in the production of various organic compounds, contributing to the synthesis of complex molecules.
Used in Materials Science:
(2-Benzylphenyl)(naphthalen-2-yl)methanone is used as a fluorescent material for the development of optical and electronic devices, taking advantage of its fluorescent properties.

Check Digit Verification of cas no

The CAS Registry Mumber 7424-65-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,2 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7424-65:
(6*7)+(5*4)+(4*2)+(3*4)+(2*6)+(1*5)=99
99 % 10 = 9
So 7424-65-9 is a valid CAS Registry Number.

7424-65-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-benzylphenyl)-naphthalen-2-ylmethanone

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

Emergency phone number -
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More Details:7424-65-9 SDS

7424-65-9Relevant academic research and scientific papers

Synthesis of 2-Benzylphenyl Ketones by Aryne Insertion into Unactivated C-C Bonds

Rao, Bin,Tang, Jinghua,Zeng, Xiaoming

supporting information, p. 1678 - 1681 (2016/04/26)

A transition-metal-free procedure to access to functionalized 2-benzylphenyl ketones is described by direct insertion of arynes into benzylic C-C bonds. This reaction was promoted by cesium fluoride at room temperature, allowing the products to form in high selectivity and achieve good functional group tolerance.

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