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2(1H)-Pyridinone, 3,4-diphenyl- is an organic compound with the chemical formula C17H13NO. It is a derivative of pyridinone, featuring two phenyl groups attached to the 3rd and 4th carbon atoms of the pyridinone ring. 2(1H)-Pyridinone, 3,4-diphenyl- is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure. It is a white crystalline solid and is typically used as an intermediate in chemical reactions. The compound's properties, such as its melting point and solubility, can be influenced by the presence of the phenyl groups, making it a versatile building block in organic synthesis.

5216-02-4

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5216-02-4 Usage

Compound type

Pyridinone derivative

Substitution

3,4-Diphenyl

Potential applications

Pharmaceutical and chemical industries (building block for synthesis of biologically active compounds), materials science (functional materials, organic electronics)

Versatility

Diverse potential applications

Interest

Subject of research and development in various fields

Check Digit Verification of cas no

The CAS Registry Mumber 5216-02-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,1 and 6 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5216-02:
(6*5)+(5*2)+(4*1)+(3*6)+(2*0)+(1*2)=64
64 % 10 = 4
So 5216-02-4 is a valid CAS Registry Number.

5216-02-4SDS

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 3,4-diphenylpyridin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 3,4-Diphenyl-pyridon-2

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 -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5216-02-4 SDS

5216-02-4Downstream Products

5216-02-4Relevant academic research and scientific papers

Substituent effects on the iodine-catalyzed thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates: Mechanistic studies

Chuang, Ta-Hsien,Chang, Wei-Yu,Li, Chien-Fu,Wen, Yu-Chia,Tsai, Chia-Chen

, p. 9678 - 9686 (2012/01/05)

The thermal cyclization of 3,4-diphenylbuta-1,3-dienyl isocyanates 1, generated in situ from the corresponding azides, was investigated using iodine as a catalyst. Diphenylpyridinones 2, phenylnaphthalenes 3, and indenes 4 were produced via intramolecular ring closure. The nature of the substituents on the phenyl rings was found to be crucial to the distribution of cyclized products 2 - 4. The mechanism of the reaction is also discussed.

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