3647-33-4 Usage
Uses
Used in Organic Chemistry:
Ethyl 2,3-anhydro-4,5-dideoxy-3-C-methylpentonate is used as a synthetic intermediate for the development of complex organic molecules. Its unique structure allows for specific reactions and modifications that can lead to the creation of novel compounds with potential applications in various fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ethyl 2,3-anhydro-4,5-dideoxy-3-C-methylpentonate is used as a key building block for the synthesis of new drug candidates. Its structural features can be exploited to design molecules with specific biological activities, potentially leading to the discovery of new therapeutic agents.
Used in Research and Development:
Ethyl 2,3-anhydro-4,5-dideoxy-3-C-methylpentonate is utilized as a research compound in academic and industrial laboratories. Its complex structure provides opportunities for studying various chemical reactions and mechanisms, contributing to the advancement of scientific knowledge and the development of new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 3647-33-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,4 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3647-33:
(6*3)+(5*6)+(4*4)+(3*7)+(2*3)+(1*3)=94
94 % 10 = 4
So 3647-33-4 is a valid CAS Registry Number.
3647-33-4Relevant academic research and scientific papers
Williams, Philip G.,Luesch, Hendrik,Yoshida, Wesley Y.,Moore, Richard E.,Paul, Valerie J.
, p. 595 - 598 (2003)
Re-collections of the cyanobacterium Lyngbya sp. have yielded two more members of the lyngbyapeptin and lyngbyabellin families. The gross structures of 15-norlyngbyapeptin A (1) and lyngbyabellin D (3) were deduced through standard 2D NMR techniques, with the absolute configuration of both elucidated through degradation and comparison with commercially available and synthetic standards. Degradation to the α-amino acid and NOE correlations determined the absolute and relative configuration of the 4-amino-3-hydroxy-5-methylhexanoic acid unit in 3. Lyngbyabellin D (3) displayed an IC50 value of 0.1 μM against the KB cell line.
Methode generale d'obtention des α-ceto esters β-fluores
Ourari, Ali,Condom, Roger,Guedj, Roger
, p. 2707 - 2710 (2007/10/02)
A general method of synthesis of 3-alkyl (or aryl) 3-fluoro 2-oxo esters is described.The opening of glycidic esters with HF-pyridine (70percent w/w) followed by oxidation with Jones reagent, give the corresponding derivatives of fluoropyruvic esters in good yields.
