19234-58-3 Usage
Description
4-Nitrophenyl2-acetamido-2-deoxy-4,6-O-benzylidene-b-D-glucopyranoside is a complex organic compound with a unique chemical structure. It is characterized by its off-white solid appearance and is primarily used in the field of organic synthesis.
Uses
Used in Organic Synthesis:
4-Nitrophenyl2-acetamido-2-deoxy-4,6-O-benzylidene-b-D-glucopyranoside is used as a synthetic intermediate for the development of various organic compounds. Its unique structure allows it to be a valuable building block in the synthesis of complex molecules, particularly in the pharmaceutical and chemical industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Nitrophenyl2-acetamido-2-deoxy-4,6-O-benzylidene-b-D-glucopyranoside is used as a key component in the development of new drugs. Its chemical properties make it suitable for the synthesis of bioactive molecules with potential therapeutic applications.
Used in Chemical Research:
4-Nitrophenyl2-acetamido-2-deoxy-4,6-O-benzylidene-b-D-glucopyranoside is also utilized in chemical research as a model compound to study various reaction mechanisms and to develop new synthetic methodologies. Its unique structure provides researchers with valuable insights into the reactivity and behavior of similar compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 19234-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,3 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19234-58:
(7*1)+(6*9)+(5*2)+(4*3)+(3*4)+(2*5)+(1*8)=113
113 % 10 = 3
So 19234-58-3 is a valid CAS Registry Number.
19234-58-3Relevant articles and documents
Syntheses of the 3- and 4-thio analogues of 4-nitrophenyl 2-acetamido-2-deoxy-β-d-gluco- and galactopyranoside
Chen, Hong-Ming,Withers, Stephen G.
, p. 2212 - 2222 (2008/02/12)
The syntheses of 4-nitrophenyl β-glycosides of the 3-thio and 4-thio analogues of the two principal 2-acetamido-2-deoxy-hexoses found in living systems, GlcNAc and GalNAc, are described. While synthesis of the 4-thio analogues could be achieved via nucleophilic displacements of sulfonate derivatives with thioacetate, problems with neighbouring group acetamido participation necessitated the use of sulfamidate intermediates for the 3-thio analogues. These 3- and 4-thio analogues are employed in the chemo-enzymatic synthesis of thio-oligosaccharide analogues of structures present in glycosaminoglycans, glycoproteins and glycolipids.
