23339-16-4 Usage
Description
Ethyl 2,3-dideoxyhexopyranoside is a unique chemical compound characterized by a six-carbon sugar backbone with an ethyl group attached to the second carbon. As a glycoside, it is formed from a simple sugar and another molecule, and it is specifically classified as a dideoxyhexopyranoside due to the absence of two hydroxyl groups compared to a standard hexopyranoside. The presence of the ethyl group imparts a hydrophobic property to the molecule, which is beneficial for various biochemical and pharmaceutical applications. This structurally distinct compound holds promise for a wide array of research and industrial uses.
Uses
Used in Biochemical Research:
Ethyl 2,3-dideoxyhexopyranoside is utilized as a research compound for studying the interactions between sugars and other biomolecules. Its unique structure allows for the investigation of carbohydrate recognition and binding processes, which are crucial for understanding various biological functions and mechanisms.
Used in Pharmaceutical Development:
In the pharmaceutical industry, ethyl 2,3-dideoxyhexopyranoside serves as a key intermediate in the synthesis of various drug candidates. Its hydrophobic nature and structural features make it a valuable component in the development of novel therapeutic agents targeting specific biological pathways or receptors.
Used in Drug Delivery Systems:
Ethyl 2,3-dideoxyhexopyranoside is employed as a component in drug delivery systems to enhance the solubility, stability, and bioavailability of pharmaceutical compounds. Its hydrophobic property can improve the encapsulation of drugs in carriers, facilitating targeted and controlled release of therapeutic agents.
Used in Chemical Synthesis:
As a versatile building block, ethyl 2,3-dideoxyhexopyranoside is used in the synthesis of a range of organic compounds, including complex carbohydrates, natural products, and other bioactive molecules. Its unique structure provides opportunities for the development of new synthetic routes and methodologies in organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 23339-16-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,3 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 23339-16:
(7*2)+(6*3)+(5*3)+(4*3)+(3*9)+(2*1)+(1*6)=94
94 % 10 = 4
So 23339-16-4 is a valid CAS Registry Number.
23339-16-4Relevant articles and documents
Synthesis of the GHIJKL Fragment of Gymnocin-B
Sakai, Takeo,Sakakibara, Hideaki,Omoto, Yumi,Tsunekawa, Marina,Hadano, Yoshinori,Kato, Shota,Mori, Yuji
, p. 6864 - 6868 (2019)
The GHIJKL fragment of gymnocin-B was synthesized using the oxiranyl anion strategy. The first highlight of the synthesis is the bromoketone cyclization reaction on the oxepane ring to construct the fused bisoxepane GH ring. The second key step is the int
Total synthesis of enantiomerically pure (-)-Balanol
Barbier, Pierre,Stadlwieser, Josef
, p. 530 - 532 (2007/10/03)
The total synthesis of enantiomerically pure (-)-Balanol (1), using tri-O-acetyl-D-glucal as a chiral template for the central azepane fragment is described.
A Mild and Simple Enzymatic Conversion of Aldono- and Aldurononitriles into the Corresponding Amides and/or Carboxylic Acids
Raadt, Anna de,Griengl, Herfried,Klempier, Norbert,Stuetz, Arnold E.
, p. 3179 - 3184 (2007/10/02)
-
