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2(3H)-Benzofuranone, 3-(4-methylphenyl)-, also known as 4-methylphenyl-3-benzofuran-2-one, is a chemical compound belonging to the benzofuranone family. It has the molecular formula C16H12O and features a benzene ring fused to a furan ring. 2(3H)-Benzofuranone, 3-(4-methylphenyl)is recognized for its diverse biological activities, such as anti-inflammatory, anti-fungal, and anti-tumor properties, which make it valuable in both medicinal and industrial applications. However, due to potential hazards to human health and the environment, it is crucial to handle this chemical with caution.

4815-06-9

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4815-06-9 Usage

Uses

Used in Pharmaceutical Industry:
2(3H)-Benzofuranone, 3-(4-methylphenyl)is used as an active pharmaceutical ingredient for its various biological activities, including its anti-inflammatory, anti-fungal, and anti-tumor properties. These characteristics make it a valuable compound in the development of new drugs and treatments for a range of health conditions.
Used in Food Industry:
In the food industry, 2(3H)-Benzofuranone, 3-(4-methylphenyl)is utilized as a flavoring agent. Its unique chemical structure contributes to the development of specific taste profiles, enhancing the sensory experience of food products. However, it is essential to ensure that the compound is used within safe limits to avoid any adverse effects on consumers.

Check Digit Verification of cas no

The CAS Registry Mumber 4815-06-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4815-06:
(6*4)+(5*8)+(4*1)+(3*5)+(2*0)+(1*6)=89
89 % 10 = 9
So 4815-06-9 is a valid CAS Registry Number.

4815-06-9Relevant academic research and scientific papers

A Concise Synthesis of 2-(2-Hydroxyphenyl)acetonitriles via the o-Quinone Methides Generated from 2-(1-Tosylalkyl)phenols

Wu, Bo,Gao, Xiang,Chen, Mu-Wang,Zhou, Yong-Gui

supporting information, p. 981 - 984 (2016/02/18)

A concise synthesis of 2-(2-hydroxyphenyl)acetonitriles has been developed through reaction of trimethylsilyl cyanide and the o-quinone methides in situ generated from 2-(1-tosylalkyl)phenols under basic conditions. In addition, 2-(2-hydroxyphenyl)acetonitriles could be conveniently transformed to benzofuranones.

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