162088-92-8 Usage
Description
2-Nitrophenyl2,2',3,3',4'-penta-O-acetyl-b-D-xylobioside is a complex organic compound that is primarily utilized in the field of organic synthesis. It is characterized by its unique chemical structure, which features a nitrophenyl group and a xylobioside moiety with multiple acetyl groups attached. 2-Nitrophenyl2,2',3,3',4'-penta-O-acetyl-b-D-xylobioside is known for its potential applications in various chemical and pharmaceutical processes due to its versatile reactivity and structural properties.
Uses
Used in Organic Synthesis:
2-Nitrophenyl2,2',3,3',4'-penta-O-acetyl-b-D-xylobioside is used as a key intermediate in organic synthesis for the development of various complex organic molecules. Its unique structure allows for a wide range of chemical reactions, making it a valuable compound for the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Nitrophenyl2,2',3,3',4'-penta-O-acetyl-b-D-xylobioside is used as a building block for the synthesis of novel drug candidates. Its structural diversity and reactivity enable the creation of new molecules with potential therapeutic properties, contributing to the discovery of innovative treatments for various diseases and conditions.
Used in Chemical Research:
2-Nitrophenyl2,2',3,3',4'-penta-O-acetyl-b-D-xylobioside is also employed in chemical research as a model compound for studying various reaction mechanisms and exploring new synthetic methodologies. Its unique structure provides researchers with an opportunity to investigate new chemical transformations and develop innovative strategies for the synthesis of complex organic molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 162088-92-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,0,8 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 162088-92:
(8*1)+(7*6)+(6*2)+(5*0)+(4*8)+(3*8)+(2*9)+(1*2)=138
138 % 10 = 8
So 162088-92-8 is a valid CAS Registry Number.
162088-92-8Relevant articles and documents
Synthesis of 2- and 4-nitrophenyl β-glycosides of β-(1 → 4)-D-xylo-oligosaccharides of dp 2-4
Takeo,Ohguchi,Hasegawa,Kitamura
, p. 231 - 244 (2007/10/03)
2- and 4-Nitrophenyl β-D-xylopyranosides (4 and 5) were transformed, via dibutyltin oxide-mediated acylation, into the corresponding 2,3-di-O-benzoyl derivatives 11 and 15. Xylobiose and xylotriose were easily isolated by charcoal column chromatography from a commercially available material and converted into the di- and trisaccharide methyl 1-thio-β-glycosides 36 and 37. The 2- and 4-nitrophenyl β-glycosides of the β-(1 → 4)-D-xylo-oligosaccharides of dp 2-4 were synthesized by N-iodosuccinimide-silver triflate-promoted condensation using 11 and 15 as the glycosyl acceptors and ethyl 1-thio-β-D-xylopyranoside triacetate 16, 36, and 37 as the glycosyl donors. Also described are an improved preparation of 4 and 5, and the synthesis of 1-naphthyl β-D-xylopyranoside, as well as an alternative approach to the 2- and 4-nitrophenyl β-xylobiosides.
