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2-tert-Butylamino-1-(4-hydroxy-3-methyl-phenyl)-ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60853-66-9

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60853-66-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60853-66-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,5 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 60853-66:
(7*6)+(6*0)+(5*8)+(4*5)+(3*3)+(2*6)+(1*6)=129
129 % 10 = 9
So 60853-66-9 is a valid CAS Registry Number.

60853-66-9Relevant academic research and scientific papers

A Combined High-Throughput Screening and Reaction Profiling Approach toward Development of a Tandem Catalytic Hydrogenation for the Synthesis of Salbutamol

Leitch, David C.,Greene, Thomas F.,O'Keeffe, Roisin,Lovelace, Thomas C.,Powers, Jeremiah D.,Searle, Andrew D.

, p. 1806 - 1814 (2017)

A combined high-throughput screening and reaction profiling approach to the telescoping of two reductions in the synthesis of Salbutamol is described. Optimization studies revealed the beneficial effect of mildly acidic conditions, and the use of water as a cosolvent. Persistent formation of deoxygenated impurities using a Pd/C catalyst led to the initiation of reaction profiling studies, which revealed that the ketone intermediate formed after rapid debenzylation is the sole source of deoxygenated impurities, indicating that more rapid ketone hydrogenation should minimize this deoxygenation. A dual catalyst approach based on these insights has been developed, with both Pd/Pt and Ru/Pt catalyst systems as more selective than Pd-only systems. Based on reaction profiles that indicate the deoxygenation side reaction is first-order in the concentration of debenzylated ketone intermediate, Pt catalysts for rapid and selective ketone hydrogenation were paired with Pd and Ru catalysts known to perform selective debenzylation. Optimization of these dual catalyst processes led to conditions that were demonstrated on 20 g scale to prepare Salbutamol in 49% isolated yield after recrystallization.

Preparation method and application of salbutamol impurity

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Paragraph 0005; 0082; 0086, (2021/06/22)

The invention discloses a preparation method and application of a salbutamol impurity. The preparation method adopts the following process route of taking 2-acetoxy-5-(2-bromoacetyl) benzyl acetate (ABBA) as an initial raw material, and firstly reacting w

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