70867-33-3 Usage
Uses
Used in Organic Synthesis:
O-NITROPHENYL BETA-D-CELLOBIOSIDE is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows chemists to exploit its reactivity in the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Analytical Chemistry:
O-NITROPHENYL BETA-D-CELLOBIOSIDE is employed as a substrate in the study and analysis of enzymatic reactions, particularly those involving cellulases and other glycoside hydrolases. The o-nitrophenyl group acts as a chromophore, providing a colorimetric assay to monitor enzyme activity and kinetics.
Used in Research and Development:
In the field of research and development, O-NITROPHENYL BETA-D-CELLOBIOSIDE serves as a valuable tool for investigating the structure, function, and mechanism of action of cellulose-degrading enzymes. It also aids in the development of new catalysts and biocatalysts for the degradation and conversion of cellulose into valuable products.
Used in Material Science:
O-NITROPHENYL BETA-D-CELLOBIOSIDE can be utilized in the development of novel materials with specific properties, such as films, coatings, and hydrogels, by exploiting its reactivity and the ability to form self-assembled structures.
Used in Environmental Applications:
In environmental applications, O-NITROPHENYL BETA-D-CELLOBIOSIDE can be employed in the development of biodegradable materials and the study of the degradation of cellulose in various ecosystems, contributing to a better understanding of the carbon cycle and waste management strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 70867-33-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,8,6 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 70867-33:
(7*7)+(6*0)+(5*8)+(4*6)+(3*7)+(2*3)+(1*3)=143
143 % 10 = 3
So 70867-33-3 is a valid CAS Registry Number.
InChI:InChI=1/C18H25NO13/c20-5-9-11(22)12(23)14(25)18(30-9)32-16-10(6-21)31-17(15(26)13(16)24)29-8-4-2-1-3-7(8)19(27)28/h1-4,9-18,20-26H,5-6H2
70867-33-3Relevant academic research and scientific papers
A novel thermophilic glycosynthase that effects branching glycosylation
Trincone,Perugino,Rossi,Moracci
, p. 365 - 368 (2007/10/03)
A novel thermophilic glycosynthase that effects branching glycosylation has been obtained by mutation of the nucleophile in the active site of the glycosidase from Sulfolobus solfataricus. Two methods for the use of this mutant are reported. (C) 2000 Elsevier Science Ltd. All rights reserved.
