Nom du produit:4-Nitrophenyl beta-D-glucopyranosiduronic acid

IUPAC Name:(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-nitrophenoxy)oxane-2-carboxylic acid

CAS:10344-94-2
Formule moléculaire:C12H13NO9
Pureté:95%
Numéro de catalogue:CM100362
Poids moléculaire:315.23

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Détails du produit

N° CAS:10344-94-2
Formule moléculaire:C12H13NO9
Point de fusion:-
Code SMILES:O[C@H]([C@H]([C@@H]([C@@H](C(O)=O)O1)O)O)[C@@H]1OC2=CC=C([N+]([O-])=O)C=C2
Densité:1.731g/cm3
Numéro de catalogue:CM100362
Poids moléculaire:315.23
Point d'ébullition:644.434°C at 760 mmHg
N° Mdl:MFCD00036210
Stockage:Store at 2-8°C.

Category Infos

Glucuronic Acid Derivatives
Glucuronic acid is a sugar acid derived from glucose, with its sixth carbon atom oxidized to a carboxylic acid.

Column Infos

Carbohydrates
Carbohydrates are polyhydroxy aldehydes (aldoses) or polyhydroxy ketones (ketoses) composed of C, H and O, or form polyhydroxy aldehydes or ketones upon hydrolysis. Carbohydrates come in the form of monosaccharides, disaccharides, oligosaccharides and polysaccharides. The simplest sugars, monosaccharides and disaccharides, consist of one or two monosaccharide units. Oligosaccharides are generally classified as carbohydrates containing 3-10 monosaccharide units. Polysaccharides contain more than 10 monosaccharide units and can be quite large. Glucose is an aldose, the most important monosaccharide in the body, used by cells as fuel. Other aldohexoses are galactose and mannose, which form part of complex molecules. Fructose is a ketohexose sugar, while ribose is the most important aldose pentose sugar and a component of RNA.


Product Other Information

Product Overview 4-Nitrophenyl beta-D-glucopyranosiduronic acid (4-NPB-D-GlcA) is a compound of a nitrophenol and a glucopyranosiduronic acid. It is a derivative of 4-nitrophenol (4-NP), which is a compound that has been used in a variety of applications, including as a dye, a preservative, and a reagent in organic synthesis. 4-NPB-D-GlcA is an important and versatile organic compound that has been studied extensively in the fields of biochemistry, organic chemistry, and biotechnology.
Synthesis and Application 4-Nitrophenyl beta-D-glucopyranosiduronic acid can be synthesized in a number of ways. One method involves the condensation of 4-nitrophenol with 1,4-dihydroxy-2-butanone in the presence of a base, such as sodium hydroxide. This reaction produces the desired product, 4-Nitrophenyl beta-D-glucopyranosiduronic acid, as well as 4-nitrobenzaldehyde and water. Another method involves the reaction of 4-nitrophenol with 1,4-dihydroxy-2-butanone in the presence of a base, such as sodium hydroxide, and a catalyst, such as sodium tetraborate. This reaction produces the desired product, 4-Nitrophenyl beta-D-glucopyranosiduronic acid, as well as 4-nitrobenzaldehyde and water. 4-Nitrophenyl beta-D-glucopyranosiduronic acid has been studied extensively in the fields of biochemistry, organic chemistry, and biotechnology. In biochemistry, it has been used as a substrate for the enzyme β-glucosidase, which is involved in the hydrolysis of glycosidic bonds. In organic chemistry, it has been used as a reagent in the synthesis of a variety of compounds, including drugs, dyes, and fragrances. In biotechnology, it has been used as a substrate for the enzyme β-glucosidase, which is involved in the hydrolysis of glycosidic bonds.
Future Directions Future research on 4-Nitrophenyl beta-D-glucopyranosiduronic acid could include further investigation into its biochemical and physiological effects, as well as its potential toxicity. It could also be studied for its potential applications in the fields of biochemistry, organic chemistry, and biotechnology. In addition, further research could be conducted to determine its potential as a drug, a dye, a preservative, or a reagent in organic synthesis. Finally, further research could be conducted to determine the mechanism of action of 4-Nitrophenyl beta-D-glucopyranosiduronic acid and its potential interactions with other compounds.