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Butanoic acid, 4-amino-3-hydroxy-, methyl ester, (3S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88759-60-8

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88759-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88759-60-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,7,5 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88759-60:
(7*8)+(6*8)+(5*7)+(4*5)+(3*9)+(2*6)+(1*0)=198
198 % 10 = 8
So 88759-60-8 is a valid CAS Registry Number.

88759-60-8Relevant academic research and scientific papers

Method for preparing levorotatory oxiracetam crystal form II through pH method

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, (2017/09/01)

The invention relates to a preparation method of a levorotatory oxiracetam crystal form II. The method comprises the steps of adopting S-4-chlorine-3-hydroxybutyrate and sodium azide as starting raw materials for preparing to obtain high-purity (S)-4-hydroxy-2 oxo-1-pyrrolidine acetamide; using acetic acid/ammonium hydroxide for preparing to obtain the (S)-4-hydroxy-2 oxo-1-pyrrolidine acetamide crystal from II through a pH method. The optical purity is 99.9 percent or above, and the product quality of the (S)-4-hydroxy-2 oxo-1-pyrrolidine acetamide crystal from II is greatly improved.

Preparation method for (S)-oxiracetam

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, (2016/12/01)

The invention provides a preparation method for (S)-oxiracetam. The preparation method comprises the following steps: (1) with S-4-chloro-3-hydroxy butyrate as an initial raw material, subjecting the initial raw material and an azido reaction agent to an azido reaction so as to obtain an intermediate I; (2) subjecting the intermediate I to a reduction reaction so as to obtain an intermediate II; (3) subjecting the intermediate II and halogenated acetate to a condensation reaction so as to obtain an intermediate III; (4) subjecting the intermediate III to a ring closure reaction so as to obtain an intermediate IV; and (4) carrying out an aminolysis reaction on the intermediate IV so as to obtain the target product (S)-oxiracetam. The preparation method can prepare the (S)-oxiracetam product with ideal yield of at least more than 38%, and a novel synthetic route is opened up for (S)-oxiracetam.

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