13264-91-0 Usage
Uses
Used in Organic Synthesis:
2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is used as a key intermediate in organic synthesis for the development of various chemical compounds. Its versatile structure enables it to be a building block for creating complex molecules with specific properties and functions.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is used as a starting material for the synthesis of novel drug candidates. Its unique chemical properties make it a promising candidate for the development of new therapeutic agents with potential applications in treating various diseases.
Used in Chemical Research:
2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside is also used in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its reactivity and structural features provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical science.
Used in Material Science:
In the field of material science, 2-Nitrophenyl2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-glucopyranoside can be used as a component in the development of new materials with specific properties. Its unique chemical structure can be exploited to create materials with tailored characteristics, such as improved stability, enhanced reactivity, or novel optical properties.
Check Digit Verification of cas no
The CAS Registry Mumber 13264-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,6 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 13264-91:
(7*1)+(6*3)+(5*2)+(4*6)+(3*4)+(2*9)+(1*1)=90
90 % 10 = 0
So 13264-91-0 is a valid CAS Registry Number.
13264-91-0Relevant academic research and scientific papers
Facile synthesis of nitrophenyl 2-acetamido-2-deoxy-α-D- mannopyranosides from ManNAc-oxazoline
Krenek, Karel,Simon, Petr,Weignerova, Lenka,Fliedrova, Barbora,Kuzma, Marek,Kren, Vladimir
, p. 428 - 432 (2012/05/05)
The synthetic procedures for a large-scale preparation of o- and p-nitrophenyl 2-acetamido-2-deoxy-α-D-mannopyranoside are described. The synthetic pathway employs the glycosylation of phenol with ManNAc oxazoline, followed by nitration of the aromatic moiety yielding a separable mixture of the o- and p-nitrophenyl derivative in a 2:3 ratio.
The use of the o-nitrophenyl group as a protecting/activating group for 2-acetamido-2-deoxyglucose
Pistia-Brueggeman, Gabriela,Hollingsworth, Rawle I.
, p. 455 - 458 (2007/10/03)
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
