146288-30-4 Usage
Description
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is a glycoside derivative of glucose, characterized by its acetylated form that enhances its stability and solubility. This complex chemical compound is frequently utilized in pharmaceutical and biochemical research, serving as a building block for the synthesis of various bioactive compounds and contributing to drug development. Its structural modifications make it a significant molecule for the study of carbohydrate chemistry and its implications in biological processes.
Uses
Used in Pharmaceutical Research:
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a key intermediate in the synthesis of pharmaceutical compounds for drug development. Its unique structure allows for the creation of new molecules with potential therapeutic properties.
Used in Biochemical Research:
In the field of biochemical research, AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a building block for the synthesis of bioactive compounds. Its acetylated form facilitates easier handling and manipulation in laboratory settings, making it an important molecule for studying carbohydrate chemistry and its role in biological processes.
Used in Drug Development:
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is employed as a precursor in the development of new drugs. Its structural modifications provide a foundation for the design of innovative pharmaceutical agents with potential applications in treating various diseases and conditions.
Used in Carbohydrate Chemistry Studies:
In the study of carbohydrate chemistry, AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used to explore the interactions between carbohydrates and other biomolecules. Its unique structure offers insights into the role of carbohydrates in biological processes and their potential applications in medicine and biotechnology.
Used in Synthesis of Bioactive Compounds:
AMYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a starting material for the synthesis of bioactive compounds with potential applications in various industries, including pharmaceuticals, cosmetics, and food science. Its versatility and stability make it an attractive candidate for the development of novel compounds with therapeutic or functional properties.
Check Digit Verification of cas no
The CAS Registry Mumber 146288-30-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,2,8 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 146288-30:
(8*1)+(7*4)+(6*6)+(5*2)+(4*8)+(3*8)+(2*3)+(1*0)=144
144 % 10 = 4
So 146288-30-4 is a valid CAS Registry Number.
146288-30-4Relevant articles and documents
Convergent synthesis of tetra- and penta-saccharide fragments of dimeric Lewis X
Forman, Adam,Hendel, Jenifer,Auzanneau, France-Isabelle
, (2019)
The convergent synthesis of tetra- and penta-saccharide fragments of the TACA dimeric Lex is described. The synthetic strategy relied on the preparation of a protected GlcNTCA-(1,3)-Gal-(1,4)-GlcNAc trisaccharide diol free at O-3 of both glucos
Use of sodium iodide and crown ether in the synthesis of N-acetylglucosamine glycosides
Kur'yanov,Zemlyakov,Chupakhina,Chirva
, p. 282 - 283 (2007/10/03)
A pair of sodium iodide-crown ether reagents was used in the synthesis of N-acetylglucosamine glycosides. At room temperature, the reaction resulted in β-glycosides, whereas at 85-90°C, it gave a mixture of anomers or α-anomer only.
A spacer-modified disaccharide as a photoaffinity reagent for the acceptor-binding area of bovine (1->4)-β-D-galactosyltransferase: comparison of its acceptor properties with those of other 2-acetamido-2-deoxy-β-D-glucopyranosides
Ats, Sandor-Csaba,Lehmann, Jochen,Petry, Stefan
, p. 125 - 139 (2007/10/02)
The spacer-modified disaccharide 1,10-di-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-azi-1,10-decanediol (10) that mimics the biantennary core heptasaccharide of N-glycoproteins has been synthesised.Compound 10 is an excellent acceptor in galactosyltransferase-catalysed galactosylation by UDP-galactose, is superior (7-8 fold) to analogues that have only one GlcNAc unit, and is an efficient photoaffinity reagent for galactosyltransferase.In the presence of UDP-Gal, no photoaffinity labelling by 10 takes place, which agrees with the mechanism of galactosyltransferase action.
