610-88-8 Usage
Uses
Used in Pharmaceutical Industry:
Tenuazonic acid copper from Alternaria A is used as an antitumor agent for its ability to inhibit protein synthesis in fibroblasts, making it a potential candidate for cancer treatment.
Used in Antiviral Applications:
Tenuazonic acid copper from Alternaria A is used as an antiviral agent due to its ability to inhibit viral replication and reduce the severity of viral infections.
Used in Antibacterial Applications:
Tenuazonic acid copper from Alternaria A is used as an antibacterial agent to combat bacterial infections and prevent the growth of harmful bacteria.
Used in Crop Protection:
Tenuazonic acid copper from Alternaria A is used in the agricultural industry as a natural pesticide to protect common edible crops from fungal infections and ensure crop yield and quality.
Check Digit Verification of cas no
The CAS Registry Mumber 610-88-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 610-88:
(5*6)+(4*1)+(3*0)+(2*8)+(1*8)=58
58 % 10 = 8
So 610-88-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H15NO3/c1-4-5(2)8-9(13)7(6(3)12)10(14)11-8/h5,8,13H,4H2,1-3H3,(H,11,14)
610-88-8Relevant academic research and scientific papers
Preparation method of tenuazonic Acid and derivative thereof
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Paragraph 0070-0071, (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.
