849207-59-6 Usage
Description
4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-β-D-galactopyranoside is a complex organic compound characterized by its unique chemical structure. It is a white solid with specific chemical properties that make it useful in various applications, particularly in organic synthesis.
Uses
Used in Organic Synthesis:
4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-β-D-galactopyranoside is used as a synthetic intermediate for the preparation of various complex organic molecules. Its unique structure allows it to serve as a building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
In the field of research and development, 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-β-D-galactopyranoside is utilized as a tool compound to study the properties and reactivity of similar complex molecules. It can also be used to develop new synthetic methods and techniques for the preparation of related compounds.
Used in Pharmaceutical Industry:
4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-β-D-galactopyranoside is used as a key intermediate in the synthesis of certain pharmaceutical agents. Its unique structure and reactivity make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Analytical Chemistry:
In analytical chemistry, 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-β-D-galactopyranoside can be employed as a derivatizing agent for the detection and quantification of specific analytes. Its unique chemical properties allow for selective reactions and enhanced detection capabilities.
Overall, 4-Methylumbelliferyl 2-Acetamido-2-deoxy-3,6-dipivaloyl-β-D-galactopyranoside is a versatile compound with a wide range of applications in various industries, including organic synthesis, pharmaceuticals, research and development, and analytical chemistry. Its unique structure and properties make it a valuable asset in the development of new molecules and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 849207-59-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,2,0 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849207-59:
(8*8)+(7*4)+(6*9)+(5*2)+(4*0)+(3*7)+(2*5)+(1*9)=196
196 % 10 = 6
So 849207-59-6 is a valid CAS Registry Number.
849207-59-6Relevant articles and documents
Dynamic combinatorial chemistry: Lysozyme selects an aromatic motif that mimics a carbohydrate residue
Zameo, Sandrine,Vauzeilles, Boris,Beau, Jean-Marie
, p. 965 - 969 (2007/10/03)
Lysozyme makes its choice: Hen egg-white lysozyme selects the optimal binder from a collection of aromatic motifs that mimic a carbohydrate unit upon exposure to a dynamic library of potential ligands that are directed towards its active site by a low-aff