33019-34-0 Usage
Uses
Used in Organic Synthesis:
2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl Salicylate is used as a synthetic intermediate for the production of various organic compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of complex molecules, particularly in the pharmaceutical and chemical industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl Salicylate is used as a key component in the development of new drugs. Its ability to form stable derivatives and interact with other molecules makes it a promising candidate for the creation of novel therapeutic agents.
Used in Chemical Research:
2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl Salicylate is also utilized in chemical research as a model compound for studying the properties and behavior of similar glucopyranosyl derivatives. This helps researchers gain a deeper understanding of the structure-activity relationships and potential applications of these compounds.
Used in Material Science:
In the field of material science, 2,3,4,6-Tetra-O-acetyl-b-D-glucopyranosyl Salicylate can be employed as a component in the development of new materials with specific properties, such as improved stability, reactivity, or biocompatibility. Its unique structure and functional groups make it a valuable addition to the toolbox of materials scientists.
Check Digit Verification of cas no
The CAS Registry Mumber 33019-34-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33019-34:
(7*3)+(6*3)+(5*0)+(4*1)+(3*9)+(2*3)+(1*4)=80
80 % 10 = 0
So 33019-34-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H24O12/c1-10(22)28-9-16-17(29-11(2)23)18(30-12(3)24)19(31-13(4)25)21(33-16)32-15-8-6-5-7-14(15)20(26)27/h5-8,16-19,21H,9H2,1-4H3,(H,26,27)/t16?,17-,18+,19+,21-/m1/s1
33019-34-0Relevant academic research and scientific papers
Synthesis of Glycosylated Chrysin Derivatives Via Ester Linkers
Fei, Gaishun,Fan, Xiaofei,Ma, Huiping,Fan, Pengchang,Jia, Zhengping,Jing, Linlin
, p. 602 - 610 (2016/08/31)
A series of glycosylated chrysin derivatives have been synthesized in good yields with simple procedures and mild reaction conditions. Six different kinds of sugar moieties were introduced through each ester linker.
Synthesis and biological evaluation of glycosylated psoralen derivatives
Chen, Chao-Yue,Sun, Jian-Guo,Liu, Fei-Yan,Fung, Kwok-Pui,Wu, Ping,Huang, Zhi-Zhen
, p. 2598 - 2606 (2012/05/20)
A novel route for the efficient synthesis of a target psoralen moiety, 4,4′-dimethylxanthotoxol, has been developed, which need only four steps using cheap pyrogallol as a starting material. Subsequently, a range of new glycosylated psoralen derivatives w
Glycopeptide Synthesis: Selective C-terminal Deblocking and Peptide Chain Elongation of Glucosylserine Derivatives
Buchholz, Michael,Kunz, Horst
, p. 1859 - 1885 (2007/10/02)
Benzyloxycarbonyl-(Z-)serine 2-bromoethyl ester (3b) reacts with 2,3,4,6-tetra-O-benzoyl-α-D-glucopyranosyl bromide (14) to give the glucosylserine ester 15.After conversion into the corresponding 2-iodoethyl ester 23 the carboxylic group is deblocked selectively by reductive elimination using zinc.In this procedure the Z and the carbohydrate protective functions as well as the sensitive O-glycoside bond remain unaffected.The glycosylserine 24 is condensed with amino acid 2-bromoethyl esters 2 to form protected glycodipeptide 2-bromoethyl esters 18 which are extended to give glycotripeptide esters 25 after selective carboxyl deblocking.Whereas protected serine dipeptides 5 are glycosylated with 14 to form the conjugates 18, the glycosylation of the serine tripeptides 10 was not successful.
