7702-22-9 Usage
Description
(2-Benzylphenyl)(4-methoxyphenyl)methanone, also known as 2,4-dimethoxybenzyl phenyl ketone, is a chemical compound that consists of a benzyl and a methoxyphenyl group attached to a ketone functional group. It is commonly used in organic synthesis as a building block for the production of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it has been studied for its potential biological activities, such as its antifungal and antibacterial properties, and has been evaluated for its potential use as a photoactive material in organic optoelectronic devices. It is also considered to have potential applications in the field of material science and organic chemistry.
Uses
Used in Pharmaceutical Industry:
(2-Benzylphenyl)(4-methoxyphenyl)methanone is used as a building block for the synthesis of various pharmaceutical compounds due to its unique chemical structure and properties.
Used in Agrochemical Industry:
(2-Benzylphenyl)(4-methoxyphenyl)methanone is used as a building block for the synthesis of agrochemicals, contributing to the development of new and effective products for agricultural applications.
Used in Organic Synthesis:
(2-Benzylphenyl)(4-methoxyphenyl)methanone is used as a key intermediate in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products.
Used in Organic Optoelectronic Devices:
(2-Benzylphenyl)(4-methoxyphenyl)methanone is used as a photoactive material in the development of organic optoelectronic devices, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs), due to its potential light-emitting and energy conversion properties.
Used in Material Science:
(2-Benzylphenyl)(4-methoxyphenyl)methanone is used in the field of material science for the development of new materials with unique properties, such as high thermal stability, electrical conductivity, or mechanical strength.
Used in Organic Chemistry Research:
(2-Benzylphenyl)(4-methoxyphenyl)methanone is used as a research compound in organic chemistry to explore its potential applications and properties, contributing to the advancement of scientific knowledge in this field.
Check Digit Verification of cas no
The CAS Registry Mumber 7702-22-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,0 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7702-22:
(6*7)+(5*7)+(4*0)+(3*2)+(2*2)+(1*2)=89
89 % 10 = 9
So 7702-22-9 is a valid CAS Registry Number.
7702-22-9Relevant articles and documents
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.
