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2-(4-chlorophenyl)-2-hydroxy-N-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10295-46-2

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10295-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10295-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10295-46:
(7*1)+(6*0)+(5*2)+(4*9)+(3*5)+(2*4)+(1*6)=82
82 % 10 = 2
So 10295-46-2 is a valid CAS Registry Number.

10295-46-2Downstream Products

10295-46-2Relevant academic research and scientific papers

Synthesis of α-Hydroxycarboxylic Acid Anilides via Copper-Catalyzed C-N Coupling of α-Hydroxyamides with Aryl Halides

Li, Zhijie,Wen, Quan,Zhou, Lihong,Deng, Xingmei,Zeng, Qingle

, p. 3751 - 3757 (2015)

The synthesis of highly important α-hydroxycarboxylic acid anilides via copper-catalyzed chemoselective C-N coupling reactions of α-hydroxyamides and aryl halides is described. This highly selective N-arylation process demonstrates wide substrate scope, c

Zirconium-MOF-catalysed selective synthesis of α-hydroxyamide via the transfer hydrogenation of α-ketoamide

Mishra, Ashish A.,Bhanage, Bhalchandra M.

, p. 6160 - 6167 (2019/04/25)

This work reports the synthesis of α-hydroxy amide and its derivatives using zirconium-based metal-organic frameworks (Zr-MOFs). The Zr-MOF was prepared using a ligand containing different functionalities as a linker with different porosities. The catalyst efficiently facilitated the transfer hydrogenation of α-ketoamide to α-hydroxyamide. The reaction involved a green hydrogen source, namely isopropyl alcohol, which also acted as a solvent. The role of the ligand in the catalyst was optimized for the selective conversion of α-ketoamide to α-hydroxyamide. UiO-66 (Zr) crystal was efficiently used for the first time for the hydrogenation of α-ketoamide to α-hydroxyamide. The catalyst was recovered and recycled five times without any loss in activity and selectivity performance. The morphology, activity and stability of the UiO-66 (Zr) catalyst were analyzed using field emission gun scanning electron microscopy (FEG-SEM), X-ray diffraction (XRD), infra-red (IR) spectroscopy and thermogravimetric analysis (TGA). The existence of α-hydroxyamide and its derivatives was confirmed from 1H and 13C-NMR.

Α-hydroxy aryl acetylmethylene aromatic amine synthesis process

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Paragraph 0008; 0009; 0014; 0015, (2016/10/10)

Alpha-hydroxy aryl acetyl arylamine can be used as medicine and organic intermediate. The invention discloses a synthetic process of alpha-hydroxy aryl acetyl arylamine. Under existence of a copper catalyst and alkali, alpha-hydroxy aryl acetamide and ary

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