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1-Propanone, 1,3-diphenyl-3-(phenylimino)-, also known as 1,3-diphenyl-3-phenyliminopropan-1-one, is an organic compound with the molecular formula C20H17NO. It is a derivative of propanone, featuring two phenyl groups attached to the carbonyl carbon and an additional phenyl group connected to the nitrogen atom through an imine bond. 1-Propanone, 1,3-diphenyl-3-(phenylimino)- is characterized by its aromatic structure and is often used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique reactivity and stability. It is typically synthesized through the condensation of benzophenone with aniline, followed by a subsequent reaction with another equivalent of aniline to form the imine. The compound is soluble in organic solvents and has a melting point of around 90-92°C.

2080-40-2

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2080-40-2 Usage

Physical properties

Yellow crystalline solid with a distinct odor

Uses

Fragrance ingredient in cosmetics and personal care products, production of pharmaceuticals, building block in organic synthesis, synthesis of chalcone derivatives for medicinal and pharmaceutical applications

Additional properties

Potential antioxidant and antimicrobial properties, making it a versatile compound with a range of potential uses in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 2080-40-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2080-40:
(6*2)+(5*0)+(4*8)+(3*0)+(2*4)+(1*0)=52
52 % 10 = 2
So 2080-40-2 is a valid CAS Registry Number.

2080-40-2Relevant academic research and scientific papers

Aktive Malonester als Synthons fuer Heterocyclen: Eine Methode zur Hertstellung von 4-Hydroxy-2(1H)-pyridonen

Kappe, Thomas,Ajili, Samir,Stadlbauer, Wolfgang

, p. 463 - 468 (2007/10/02)

4-Hydroxy-2-(1H)-pyridones 3 can be obtained in excellent yields from azomethines 1 with trichlorophenylmalonates 2.The variation of the substituents in position 1,3,5 or 6, respectively is possible over a wide range.In this manner the 5,6-fused-pyridones

Acylsilanes and C-Stannylimines as Anion Equivalents

Degl'Innocenti, Alessandro,Pike, Stephen,Walton, David R. M.,Seconi, Giancarlo,Ricci, Alfredo,Fiorenza, Mariella

, p. 1201 - 1202 (2007/10/02)

Acylsilanes and C-stannylimines react with organic halides in the presence of KF-18-crown-6 ether to give ketones and ketimines, respectively.

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