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diethyl (tricyclo[3.3.1.1~3,7~]dec-1-ylcarbonyl)propanedioate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33566-13-1

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33566-13-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33566-13-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,6 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 33566-13:
(7*3)+(6*3)+(5*5)+(4*6)+(3*6)+(2*1)+(1*3)=111
111 % 10 = 1
So 33566-13-1 is a valid CAS Registry Number.

33566-13-1Downstream Products

33566-13-1Relevant academic research and scientific papers

Preparation method of 1-adamantyl methy ketone

-

, (2019/06/08)

The invention belongs to the field of preparation of chemical intermediates, and particularly relates to a preparation method of 1-adamantyl methy ketone. The preparation method comprises the following steps of step 1, enabling adamantane and liquid bromine to react, so as to obtain 1-bromoadamantane; step 2, using concentrated sulfuric acid as a catalyst, adding the 1-bromoadamantane and n-hexane, and dripping formic acid, so as to obtain 1-adamantanecarboxylic acid; step 3, enabling the 1-adamantanecarboxylic acid and thionyl chloride to react, heating and refluxing, extracting by benzene, and directly applying the extracting liquid for the reaction in next step; step 4, dripping a mixed solution of benzene, diethyl malonate and anhydrous ethyl alcohol into a mixed solution of magnesiumpowder, iodine, anhydrous ethyl alcohol and benzene, dripping a benzene solution of 1-adamantanecarbonyl chloride, extracting by benzene, drying and distilling, so as to obtain 2- adamantanecarbonyl diethyl malonate; step 5, adding glacial acetic acid, water and concentrated sulfuric acid into the residue. The preparation method has the advantage that the yield rate is high.

Preparation of 2-(3-hydroxy-1-adamantyl)-2-oxoacetic acid: A key intermediate for saxagliptin

Li, Jingke,Zhang, Shurong,Zhou, Hongrui,Peng, Jun,Feng, Yue,Hu, Xiangnan

experimental part, p. 347 - 350 (2012/09/08)

An optimized synthetic approach to prepare 2-(3-hydroxy-1-adamantyl)-2- oxoacetic acid has been reported in a good yield under mild experimental conditions. It was synthesized from 1-adamantanecarboxylic acid via successful reaction with thionyl chloride and sodium diethyl malonate to give dimethyl (1-adamantylcarbonyl) malonate, which was subjected to hydrolysis and decarboxylation by a mixture of acetic acid with water and sulfuric acid and then oxidation by potassium permanganate. The synthesized adamantane derivative was utilized to saxagliptin.

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