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2H-Pyrrol-2-one, 3-acetyl-1,5-dihydro-4-hydroxy-5-methyl-, (S)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

128948-45-8

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128948-45-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 128948-45-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,9,4 and 8 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 128948-45:
(8*1)+(7*2)+(6*8)+(5*9)+(4*4)+(3*8)+(2*4)+(1*5)=168
168 % 10 = 8
So 128948-45-8 is a valid CAS Registry Number.

128948-45-8Downstream Products

128948-45-8Relevant academic research and scientific papers

Amic acid derivative as well as preparation method and application thereof

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Paragraph 0117; 0156-0157; 0160; 0167, (2021/09/21)

The invention provides an amine acid derivative as well as a preparation method and application thereof. The amine acid derivative has the structure as follows. Herein, R is selected from methyl, methoxy and the like. R1 Selected from C1 - C4 a

Preparation method of tenuazonic Acid and derivative thereof

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Paragraph 0121-0122, (2021/05/12)

The invention provides a preparation method of tenuazonic Acid and a derivative thereof. The synthesis route comprises the following steps: reacting malonic acid cycloisopropylidene ester with acyl chloride, then reacting with amino acid methyl ester hydr

Tetramic Acid Chemistry. Part 1. Reinvestigation of Racemisation during the Synthesis of Tetramic Acids via Dieckmann Cyclisation

Poncet, Joel,Jouin, Patrick,Castro, Bertrand,Nicolas, Louisette,Boutar, Mohamed,Gaudemer, Alain

, p. 611 - 616 (2007/10/02)

Epimerisation during the synthesis of tetramic acids by Dieckmann cyclisation of the corresponding chiral N-acyl-α-amino esters was investigated.In the case of the isoleucine derivative, the extent of epimerisation was directly evaluated by 1H NMR analysis of the 3-acylated tetramic acids (3a,b) and (5a).A chemical correlation was carried out in the case of the 5-benzyl derivative (8h).The moderate overall yield and the partial epimerisation at position C-5 limit the usefulness of this approach for tetramic acid preparation.

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