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1-Propanone, 1-(4-chlorophenyl)-3-[(3-chlorophenyl)amino]-3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136848-63-0

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136848-63-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136848-63-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,8,4 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 136848-63:
(8*1)+(7*3)+(6*6)+(5*8)+(4*4)+(3*8)+(2*6)+(1*3)=160
160 % 10 = 0
So 136848-63-0 is a valid CAS Registry Number.

136848-63-0Downstream Products

136848-63-0Relevant academic research and scientific papers

SnCl2-catalyzed three-component one-pot Mannich-type reaction: Efficient synthesis of β-aminocarbonyl compounds

Wang, Min,Song, Zhi-Guo,Wan, Xin,Zhao, Suang

, p. 1205 - 1208 (2009)

SnCl2-catalyzed three-component one-pot Mannich reaction of acetophenone or p-chloroacetophenone with different aromatic aldehydes and aromatic amines in ethanol at ambient temperature gave the corresponding β-aminocarbonyl compounds in good to excellent yields. Four new compounds are reported for the first time.

New synthesis of β -anilinochalcones by regioselective oxidation of β -anilinodihydrochalcones using iodine-DMSO

Nawghare, Beena R.,Lokhande, Pradeep D.

supporting information, p. 3287 - 3295 (2015/10/12)

β-Anilinodihydrochalcones readily undergo oxidation α to the carbonyl group region in the presence of a catalytic amount of iodine in dimethyl sulfoxide at 130 °C in good yield. Oxidation of allyloxy-substituted β-anilinodihydrochalcones to β-anilinochalcones is a preferred reaction over deallylation.

SnCl45H2O-catalyzed synthesis of β-amino carbonyl compounds via a direct Mannich-type reaction

Wang, Min,Song, Zhiguo,Liang, Yan

experimental part, p. 1 - 6 (2011/12/22)

An efficient three-component, one-pot synthesis of β-amino carbonyl compounds from aromatic ketones, aromatic aldehydes, and aromatic amines using tin tetrachloride at room temperature in ethanol is described. The advantages of the new method are good yields (62-96%), simple workup, and inexpensive catalyst. Copyright Taylor & Francis Group, LLC.

Aluminium nitrate as an efficient and reusable catalyst for the three components one-pot Mannich reaction: Synthesis of β-amino carbonyl compounds

Wang, Min,Liang, Yan,Song, Zhiguo

supporting information; experimental part, p. 1653 - 1656 (2011/02/21)

Three components one-pot Mannich reaction of aromatic ketones, aromatic aldehydes and aromatic amines has been efficiently catalysed by recyclable aluminium nitrate at ambient temperature to give various β-amino carbonyl compounds in high yields. By simple phase separation, aluminium nitrate could be recycled several times without distinct loss of activity.

The Mannich reaction between aromatic ketones, aromatic aldehydes and aromatic amines

Lin,Huangshu,Junhua,Xiujuan

, p. 717 - 718 (2007/10/02)

The acid-catalyzed Mannich reaction of acetophenones with benzaldehyde derivatives and aromatic amines gives 1,3-diaryl-3-(arylamino)propanones in high yield.

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