4-Nitrophenyl-alpha-D-penta-(1->4)-glucopyranoside, with the CAS number 66068-38-0, is a synthetic glycoside that serves as a substrate for various enzymatic reactions, particularly in the study of glycosidases. This compound features a 4-nitrophenyl group, which provides a chromogenic property, allowing for easy detection and quantification in biochemical assays. The alpha-D-penta-(1->4)-glucopyranoside structure indicates that it consists of a glucose moiety linked through alpha-(1->4) glycosidic bonds, forming a polysaccharide-like structure. Its solubility in water and organic solvents varies, making it useful in different experimental conditions. The presence of the nitrophenyl group not only enhances its reactivity but also contributes to its stability under various pH conditions. This compound is often utilized in research settings to investigate enzyme kinetics and mechanisms, particularly in the context of carbohydrate-active enzymes. Overall, its unique structural features and functional properties make it a valuable tool in biochemical and enzymatic studies.

4-nitrophenyl-alpha-D-penta-(1->4)-gluco pyranoside

66068-38-0: 4-Nitrophenyl-alpha-D-penta-(1->4)-glucopyranoside, with the CAS number 66068-38-0, is a synthetic glycoside that serves as a substrate for various enzymatic reactions, particularly in the study of glycosidases. This compound features a 4-nitrophenyl group, which provides a chromogenic property, allowing for easy detection and quantification in biochemical assays. The alpha-D-penta-(1->4)-glucopyranoside structure indicates that it consists of a glucose moiety linked through alpha-(1->4) glycosidic bonds, forming a polysaccharide-like structure. Its solubility in water and organic solvents varies, making it useful in different experimental conditions. The presence of the nitrophenyl group not only enhances its reactivity but also contributes to its stability under various pH conditions. This compound is often utilized in research settings to investigate enzyme kinetics and mechanisms, particularly in the context of carbohydrate-active enzymes. Overall, its unique structural features and functional properties make it a valuable tool in biochemical and enzymatic studies.

CAS 66068-38-0

4-nitrophenyl-alpha-D-penta-(1->4)-gluco pyranoside

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Ref: TR-N494325

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