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(Z)-3-{2-[(Z)-1-methyl-3-oxo-3-phenyl-1-propenylamino]ethyl amino}-1-phenyl-2-buten-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56570-49-1

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56570-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56570-49-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,7 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56570-49:
(7*5)+(6*6)+(5*5)+(4*7)+(3*0)+(2*4)+(1*9)=141
141 % 10 = 1
So 56570-49-1 is a valid CAS Registry Number.

56570-49-1Downstream Products

56570-49-1Relevant academic research and scientific papers

P2O5/SiO2 as a new, efficient, and reusable catalyst for preparation of β-enaminones under solvent-free conditions

Mohammadizadeh, Mohammad R.,Hasaninejad,Bahramzadeh,Khanjarlou, Z. Sardari

, p. 1152 - 1165 (2009)

P2O5/SiO2 (30% w/w) was applied as an efficient, heterogeneous, and reusable catalyst for the synthesis of β-enaminones. The reactions were rapidly completed at 80°C under solvent-free conditions and products were obtained in good to excellent yields. Copyright Taylor & Francis Group, LLC.

Fe(HSO4)3·SiO2 as an efficient, heterogeneous and recyclable catalyst for the synthesis of bis-(β-enaminones) and bis-(β-enamino esters)

Eshghi, Hossein,Safaei, Elham,Mohamad Seyedi, Seyed,Eshghi, Tahereh

, p. 1088 - 1093 (2015/02/05)

Fe(HSO4)3·SiO2 is used to catalyze the condensation of b-diketones and b-keto esters with aromatic and aliphatic diamines in solvent-free conditions at room temperature. This afforded the corresponding bis-(β-enaminones) a

Enamination of β-dicarbonyl compounds with amines

Khodaei,Khosropour,Cardel

scheme or table, p. 217 - 221 (2009/04/06)

Enamination of a wide variety of primary amines was successfully described with excellent chemoselectivity in the presence of catalytic amounts of β-cyclodextrin in water under mild conditions. Aliphatic amines also reacted efficiently to produce the corresponding enaminones.

A novel enamination of β-dicarbonyl compounds catalyzed by Bi(TFA)3 immobilized on molten TBAB

Khodaei, Mohammad M.,Khosropour, Ahmad R.,Kookhazadeh, Mehdi

, p. 209 - 212 (2007/10/03)

Enamination of a wide variety of primary amines was successfully carried out in the presence of catalytic amounts of bismuth(III) trifluoroacetate immobilized on molten tetrabutylammonium bromide as "green" media under mild conditions. This new system of the catalyst is recyclable and reusable. Generally, the results of the reaction in tetrabutylammonium bromide is better than the previously obtained results in water because of their yields and reaction times.

A mild, efficient and environmentally friendly method for the regio- and chemoselective synthesis of enaminones using Bi(TFA)3 as a reusable catalyst in aqueous media

Khosropour, Ahmad R.,Khodaei, Mohammad M.,Kookhazadeh, Mehdi

, p. 1725 - 1728 (2007/10/03)

Bismuth(III) trifluoroacetate has been found to be an extremely efficient catalyst for the preparation of β-enaminones in water. In addition, by employing this catalyst, high regio- and chemoselective enamination of carbonyl compounds was achieved.

Volatility Studies of Metal Chelates. V. Stability and Volatility of Transition Metal Chelates of Tetradentate Schiff Bases

Dilli, Sergio,Patsalides, Emilios

, p. 1579 - 1591 (2007/10/02)

A study of the effect of substituent groups on the thermal stability and volatility of 15 tetradentate β-keto enamines and various copper(II), nickel(II), palladium(II), cobalt(II), and oxovanadium(IV) derivatives has been made by employing simultaneous t

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