13089-26-4 Usage
Uses
Used in Organic Synthesis:
(2'-NITRO)PHENYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a synthetic intermediate for the production of various biologically active compounds. Its unique structure allows for further functionalization and modification, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2'-NITRO)PHENYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is used as a key component in the development of novel drug candidates. Its structural diversity and reactivity enable the creation of new molecules with potential therapeutic applications, such as antibiotics, antiviral agents, and anticancer drugs.
Used in Research and Development:
(2'-NITRO)PHENYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE is also utilized in research and development laboratories for the study of various chemical reactions and processes. Its unique structure provides researchers with opportunities to explore new synthetic routes, reaction mechanisms, and the development of innovative catalysts and reagents.
Used in Material Science:
In the field of material science, (2'-NITRO)PHENYL-2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSIDE can be employed as a component in the design and synthesis of advanced materials with specific properties, such as improved biocompatibility, enhanced stability, or targeted drug delivery capabilities.
Check Digit Verification of cas no
The CAS Registry Mumber 13089-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,8 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13089-26:
(7*1)+(6*3)+(5*0)+(4*8)+(3*9)+(2*2)+(1*6)=94
94 % 10 = 4
So 13089-26-4 is a valid CAS Registry Number.
13089-26-4Relevant academic research and scientific papers
Pistia-Brueggeman, Gabriela,Hollingsworth, Rawle I.
, p. 455 - 458 (2003)
The o-nitrophenyl group, a protecting group with latent activation potential, was used as a protecting group for the glycosidic position. It is stable to common conditions used in synthesis and can be activated for displacement and glycoside formation by an alcohol, using zinc chloride as a catalyst. Good to excellent yields of β-glycosides of the important amino sugar N-acetylglucosamine were obtained. A mechanism for the reaction is proposed.
Synthesis of N-Acetylglucosamine Aryl β-Glycosides Catalyzed by Crown Compounds
Kur'yanov,Chupakhina,Zemlyakov,Kotlyar,Kamalov,Chirva
, p. 385 - 389 (2007/10/03)
Glycosylation of various phenols with α-D-glucosaminyl chloride peracetate in a solid phase-liquid system catalyzed by crown compounds was studied. The highest yields of aryl β-glycosides were observed at room temperature in acetonitrile using anhydrous p
