38229-74-2 Usage
Uses
Used in Pharmaceutical Industry:
4'-BROMOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE is used as a biologically active compound for its ability to inhibit the bioluminescence of marine bacteria. This property makes it a promising candidate for the development of new antimicrobial agents, particularly against bacteria that rely on bioluminescence for survival or communication.
Additionally, the deacylated form of 4'-BROMOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE may have potential applications in the development of novel therapeutics, as it retains the biological activity of the parent molecule while potentially exhibiting improved pharmacokinetic properties.
Used in Research and Development:
In the field of research and development, 4'-BROMOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE can be utilized as a starting material or a key intermediate in the synthesis of various complex carbohydrates and glycoconjugates. Its unique structure and functional groups make it an attractive candidate for the development of new bioactive molecules with potential applications in various therapeutic areas.
Furthermore, 4'-BROMOPHENYL 2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-B-D-GLUCOPYRANOSIDE can be employed in the study of carbohydrate recognition and binding events, which are essential for numerous biological processes, including cell adhesion, immune response, and signal transduction. Understanding the interactions between carbohydrates and their binding partners can lead to the discovery of new therapeutic targets and the development of innovative drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 38229-74-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,2 and 9 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 38229-74:
(7*3)+(6*8)+(5*2)+(4*2)+(3*9)+(2*7)+(1*4)=132
132 % 10 = 2
So 38229-74-2 is a valid CAS Registry Number.
38229-74-2Relevant academic research and scientific papers
Preparation and characterization of glycopolymers with biphenyl spacers: Via Suzuki coupling reaction
Seto, Hirokazu,Tono, Takumi,Nagaoka, Akiko,Yamamoto, Mai,Hirohashi, Yumiko,Shinto, Hiroyuki
supporting information, p. 4474 - 4477 (2021/05/31)
Poly(vinylbiphenyl)s bearing glycoside ligands at the side chains were prepared using the Suzuku coupling reaction. Effects of glycoside reactant concentration, halide species, glycoside species, and catalyst species on the incorporation of glycoside ligand into the polymer were investigated. The obtained glycopolymers exhibited specific binding to proteins corresponding to the glycoside ligands. In addition, the biphenyl spacers formed by the Suzuki coupling reaction in the glycopolymer were fluorescent, whereas the polymer precursor was not.
Carbohydrate protein interactions. Syntheses of agglutination inhibitors of wheat germ agglutinin by phase transfer catalysis
Roy, Rene,Tropper, Francois D.
, p. 817 - 821 (2007/10/02)
Starting from chloride 1, a series of para-substituted aryl 2-acetamido-2-deoxy-β-D-glucopyranosides were prepared using phase transfer catalysis conditions with tetrabutylammonium hydrogen sulfate in 1 M sodium hydroxide and methylene chloride at room temperature.Zemplen de-O-acetylation afforded the unprotected glycosides.Optimization of reaction conditions was evaluated.Several functional group manipulations were effected to widen the number and nature of the para-substituents. Key words: phase transfer catalysis, aryl 2-acetamido-2-deoxy-β-D-glucopyranosides.
