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3-anilino-1,5-diphenyl-5H-pyrrol-2-one is a complex organic compound with the molecular formula C23H18N2O. It is characterized by a pyrrolone core, which is a type of pyrrole derivative with a carbonyl group at the 2-position. The molecule features an anilino group (an amino group attached to a phenyl ring) at the 3-position and two phenyl rings at the 1 and 5 positions. 3-anilino-1,5-diphenyl-5H-pyrrol-2-one is known for its potential applications in the field of pharmaceuticals and materials science, particularly as a building block for the synthesis of more complex molecules with specific biological activities. Its chemical structure endows it with unique electronic and steric properties, which can be exploited in the design of new drugs or functional materials.

5468-12-2

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5468-12-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5468-12-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5468-12:
(6*5)+(5*4)+(4*6)+(3*8)+(2*1)+(1*2)=102
102 % 10 = 2
So 5468-12-2 is a valid CAS Registry Number.
InChI:InChI=1/C22H18N2O/c25-22-20(23-18-12-6-2-7-13-18)16-21(17-10-4-1-5-11-17)24(22)19-14-8-3-9-15-19/h1-16,21,23H/t21-/m1/s1

5468-12-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-anilino-1,2-diphenyl-2H-pyrrol-5-one

1.2 Other means of identification

Product number -
Other names 3-anilino-1,5-diphenyl-1,5-dihydro-pyrrol-2-one

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:5468-12-2 SDS

5468-12-2Relevant academic research and scientific papers

Recyclable fluorous organocatalysts promoted three-component reactions of pyruvate, aldehyde and amine at room temperature

Qian, Jin-Long,Yi, Wen-Bin,Cai, Chun

supporting information, p. 7100 - 7102 (2013/12/04)

A new fluorous imine carbothioate has been prepared as an organocatalyst for the synthesis of pyrrol-2-ones via the cyclo-condensation reaction of aldehydes, amines, and pyruvate at room temperature. The fluorous catalyst can be easily recovered from the reaction mixture by simple fluorous solid-phase extraction (F-SPE) and used for next run reaction without further purification.

Organocatalytic three-component reactions of pyruvate, aldehyde and aniline by hydrogen-bonding catalysts

Li, Xin,Deng, Hui,Luo, Sanzhong,Cheng, Jin-Pei

experimental part, p. 4350 - 4356 (2009/04/11)

Hydrogen-bonding catalysts have been found to catalyze one-pot three-component reactions of pyruvate, anilines and aldehydes to afford versatile 3-amino-1,5-dihydro-2H-pyrrol-2-ones in high yields. Both, thioureas and phosphoric acids are viable catalysts

FIVE-MEMBERED 2,3-DIOXOHETEROCYCLES. I. SYNTHESIS AND STRUCTURE OF 1,5-DIARYLTETRAHYDRO-2,3-PYRROLEDIONES

Andreichikov, Yu. S.,Gein, V. L.,Ivanenko, O. I.,Maslivets A. N.

, p. 1983 - 1988 (2007/10/02)

Ethyl pyruvate reacts with Schiff bases to form 1,5-diaryl-3-arylamino-2,5-dihydro-2-pyrrolones, which are hydrolyzed by concentrated hydrochloric acid to 1,5-diaryltetrahydro-2,3-pyrrolediones.Pyrrolediones containing electron-donating substituents in th

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