102717-17-9 Usage
Description
p-Nitrophenyl 3-O-Benzoyl-4,6-cyclohexylidene-β-D-mannopyranoside, with the chemical abstracts service number 102717-17-9, is a pale yellow solid compound that plays a significant role in organic synthesis. It is a derivative of D-mannopyranoside, a monosaccharide, with a benzoyl group at the 3-O position and a cyclohexylidene ring at the 4,6 positions, along with a p-nitrophenyl group attached. This unique structure endows it with specific chemical properties that make it valuable in various applications.
Uses
Used in Organic Synthesis:
p-Nitrophenyl 3-O-Benzoyl-4,6-cyclohexylidene-β-D-mannopyranoside is used as a synthetic intermediate for the preparation of various complex organic molecules. Its unique structure allows for selective reactions and modifications, making it a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
In the field of research and development, this compound serves as a valuable tool for studying the properties and reactivity of complex carbohydrates and their derivatives. It can be used to investigate the mechanisms of enzymatic reactions involving sugars, as well as to develop new methods for the synthesis of glycoconjugates and other carbohydrate-based compounds.
Used in Analytical Chemistry:
p-Nitrophenyl 3-O-Benzoyl-4,6-cyclohexylidene-β-D-mannopyranoside can be employed as a chromogenic substrate in analytical chemistry, particularly for the detection and quantification of enzymes that act on carbohydrates. The p-nitrophenyl group, upon enzymatic cleavage, releases a chromophore that can be easily measured spectrophotometrically, providing a sensitive and reliable assay for enzyme activity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, p-Nitrophenyl 3-O-Benzoyl-4,6-cyclohexylidene-β-D-mannopyranoside may be utilized as a precursor for the development of novel drug candidates targeting carbohydrate-related diseases, such as diabetes, obesity, and certain types of cancer. Its unique structure can be exploited to design inhibitors or activators of specific carbohydrate-processing enzymes, potentially leading to the discovery of new therapeutic agents.
Used in Material Science:
p-Nitrophenyl 3-O-Benzoyl-4,6-cyclohexylidene--D-mannopyranoside may also find applications in material science, particularly in the development of carbohydrate-based polymers and materials with specific properties, such as biocompatibility, biodegradability, and recognition capabilities. Its ability to form stable complexes with other molecules can be harnessed to create new materials with tailored properties for various applications, including drug delivery, sensors, and coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 102717-17-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,7,1 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 102717-17:
(8*1)+(7*0)+(6*2)+(5*7)+(4*1)+(3*7)+(2*1)+(1*7)=89
89 % 10 = 9
So 102717-17-9 is a valid CAS Registry Number.
102717-17-9Relevant articles and documents
p-Trifluoroacetamidophenyl O-alpha-D-mannopyranosyl-(1----3)-O-[alpha-D-mannopyranosyl- (1----6)]-beta-D-mannopyranoside.
Ekborg,Glaudemans
, p. 213 - 221 (2007/10/02)
p-Nitrophenyl 2-O-benzyl-4,5-O-cyclohexylidene-beta-D-mannopyranoside (4) was condensed with tetra-O-benzoyl-alpha-D-mannopyranosyl bromide. The resulting, protected disaccharide was converted into p-nitrophenyl O-(2,3,4-tri-O-benzoyl-alpha-D-mannopyranos
