259143-52-7 Usage
Uses
Used in Organic Synthesis:
4-Nitrophenyl 2-Acetamido-2-deoxy-4-O-α-L-fucopyranosyl)-β-D-glucopyranoside is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows it to be a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals that require its specific functional groups and stereochemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Nitrophenyl 2-Acetamido-2-deoxy-4-O-α-L-fucopyranosyl)-β-D-glucopyranoside is utilized as a precursor in the development of new drugs. Its ability to be modified and incorporated into larger molecular frameworks makes it a promising candidate for the synthesis of innovative therapeutic agents.
Used in Research and Development:
4-NITROPHENYL 2-ACETAMIDO-2-DEOXY--4-O-A-L-FUCOPYRANOSYL)-B-D-GLUCOPYRANOSIDE also serves a vital role in research and development settings, where it can be used to study the properties and reactions of complex organic molecules. It may be employed in academic and industrial laboratories to explore new reaction pathways, test synthetic methodologies, and develop novel applications.
Used in Analytical Chemistry:
4-Nitrophenyl 2-Acetamido-2-deoxy-4-O-α-L-fucopyranosyl)-β-D-glucopyranoside can be utilized in analytical chemistry as a reference material or standard for the development and validation of analytical methods. Its distinct chemical properties make it suitable for use in high-performance liquid chromatography (HPLC), mass spectrometry, and other analytical techniques.
Check Digit Verification of cas no
The CAS Registry Mumber 259143-52-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,1,4 and 3 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 259143-52:
(8*2)+(7*5)+(6*9)+(5*1)+(4*4)+(3*3)+(2*5)+(1*2)=147
147 % 10 = 7
So 259143-52-7 is a valid CAS Registry Number.
259143-52-7Relevant academic research and scientific papers
Glycosynthase with broad substrate specificity-an efficient biocatalyst for the construction of oligosaccharide library
Wei, Jinhua,Lv, Xun,Lue, Yang,Yang, Gangzhu,Fu, Lifeng,Yang, Liu,Wang, Jianjun,Gao, Jianhui,Cheng, Shuihong,Duan, Qian,Jin, Cheng,Li, Xuebing
, p. 2414 - 2419 (2013/05/23)
A versatile glycosynthase (TnG-E338A) with strikingly broad substrate scope has been developed from Thermus nonproteolyticus β-glycosidase (TnG) by using site-directed mutagenesis. The practical utility of this biocatalyst has been demonstrated by the facile generation of a small library containing various oligosaccharides and a steroidal glycoside (total 25 compounds) in up to 100 % isolated yield. Moreover, an array of eight gluco-oligosaccharides has been readily synthesized by the enzyme in a one-pot, parallel reaction, which highlights its potential in the combinatorial construction of a carbohydrate library that will assist glycomic and glycotherapeutic research. Significantly, the enzyme provides a means by which glycosynthase technology may be extended to combinatorial chemistry.
Glycosidase-catalyzed synthesis of fucosyl di- and trisaccharide derivatives using α-L-fucosidase from Alcaligenes sp.
Zeng, Xiaoxiong,Murata, Takeomi,Usui, Taichi
, p. 309 - 316 (2007/10/03)
p-Nitrophenyl glycosides of di-and trisaccharides containing a (1→2)-, (1→3)-, (1→4)-, or (1→6)-linked α-L-fucosyl group were synthesized using the transglycosylation reaction mediated by α-L-fucosidase from Alcaligenes sp. with p-nitrophenyl glycosides of N-acetyllactosamine, lactose, D-GlcNAc, and D-Glc as acceptors. The enzymatic process for preparing these compounds is simple, and the yield is sufficiently high to make the method practical.
