93979-06-7 Usage
Uses
Used in Organic Synthesis:
4-Nitrophenyl 3-O-(α-D-Mannopyranosyl)-α-D-mannopyranoside is used as a synthetic intermediate for the preparation of various complex organic molecules. Its unique structure allows it to be a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals that require specific functional groups and stereochemistry.
Used in Research and Development:
In the field of research and development, 4-NITROPHENYL 3-O-(A-D-MANNOPYRANOSYL)-A-D-MANNOPYRANOSIDE serves as a valuable tool for studying the properties and reactions of complex carbohydrates and their derivatives. It can be used to investigate enzymatic processes, such as glycosylation reactions, and to develop new methods for the synthesis of carbohydrate-based compounds.
Used in Analytical Chemistry:
4-Nitrophenyl 3-O-(α-D-Mannopyranosyl)-α-D-mannopyranoside can also be employed in analytical chemistry as a chromogenic substrate for the detection and quantification of certain enzymes, particularly glycosidases. The nitrophenyl group acts as a reporter, changing color upon enzymatic cleavage, which allows for the easy monitoring of enzymatic activity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-NITROPHENYL 3-O-(A-D-MANNOPYRANOSYL)-A-D-MANNOPYRANOSIDE may be utilized in the development of new drugs, particularly those targeting carbohydrate-based therapeutics. Its ability to mimic natural glycoconjugates makes it a promising candidate for the design of glycomimetics and other carbohydrate-based drugs with potential applications in treating various diseases.
Used in Material Science:
4-Nitrophenyl 3-O-(α-D-Mannopyranosyl)-α-D-mannopyranoside can also find applications in material science, where it may be used to create new types of materials with specific properties. For instance, its incorporation into polymers or other materials could lead to the development of advanced materials with tailored characteristics for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 93979-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93979-06:
(7*9)+(6*3)+(5*9)+(4*7)+(3*9)+(2*0)+(1*6)=187
187 % 10 = 7
So 93979-06-7 is a valid CAS Registry Number.
InChI:InChI=1/C18H25NO13/c20-5-9-11(22)13(24)14(25)17(30-9)32-16-12(23)10(6-21)31-18(15(16)26)29-8-3-1-7(2-4-8)19(27)28/h1-4,9-18,20-26H,5-6H2
93979-06-7Relevant academic research and scientific papers
Creation of an α-mannosynthase from a broad glycosidase scaffold
Yamamoto, Keisuke,Davis, Benjamin G.
supporting information; experimental part, p. 7449 - 7453 (2012/09/21)
α-Mannosides made easy: Mutation of a family-GH31 α-glucosidase that displays plasticity to alterations at the 2-OH position of donor substrates created an efficient α-mannoside-synthesizing biocatalyst. A simple fluoride donor reagent was used for the synthesis of a range of mono-α-mannosylated conjugates using the α-mannosynthase displaying low (unwanted) oligomerization activity. Copyright
p-NITROPHENYL 2-, AND 3-O-α-D-MANNOPYRANOSYL-α-D-MANNOPYRANOSIDE
Ekborg, Goeran,Glaudemans, Cornelis P. J.
, p. 83 - 88 (2007/10/02)
p-Nitrophenyl 3- and 2-O-benzoyl-4,6-O-benzylidene-α-D-mannopyranoside were each condensed with 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl bromide, and the products were deprotected, to yield, respectively, p-nitrophenyl 2- and 3-O-mannopyranosyl-α-D-mann
