Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
27817
CAS Number:
18918-31-5
4-Nitrofenil-α-L-ramnósido
Purity:
≥ 99 % (HPLC)
Synonym(s):
p- Nitrofenil 6-desoxi-α-L-manopiranósido
Documents
$141.41 /100 mg
Tamaño
Request Bulk Quote
Product Information

4-Nitrophenyl-a-L-rhamnoside is a versatile glycoside that serves as a valuable tool in various fields, particularly in biochemical research and pharmaceutical applications. This compound is recognized for its role as a substrate in enzyme assays, where it can be utilized to study glycosidase activity. Its unique structure, featuring a nitrophenyl group, enhances its reactivity and makes it an excellent candidate for probing enzymatic mechanisms. Additionally, 4-Nitrophenyl-a-L-rhamnoside can be employed in the synthesis of more complex molecules, contributing to the development of novel therapeutics and agrochemicals.

Researchers and industry professionals appreciate the compound's stability and solubility in aqueous environments, which facilitate its use in biological assays. Its ability to release rhamnose upon hydrolysis allows for the exploration of carbohydrate metabolism and interactions in various biological systems. With its specific applications in enzyme kinetics and synthetic chemistry, 4-Nitrophenyl-a-L-rhamnoside stands out as a crucial reagent for advancing scientific knowledge and innovation in the chemical and pharmaceutical industries.

Synonyms
p- Nitrofenil 6-desoxi-α-L-manopiranósido
CAS Number
18918-31-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H15Nº7
Molecular Weight
285.25
MDL Number
MFCD00069788
PubChem ID
3388422
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
p- Nitrofenil 6-desoxi-α-L-manopiranósido
CAS Number
18918-31-5
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H15Nº7
Molecular Weight
285.25
MDL Number
MFCD00069788
PubChem ID
3388422
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Nitrophenyl-a-L-rhamnoside is widely utilized in research focused on:

  • Glycosylation Studies: This compound serves as a substrate in enzymatic reactions to study glycosylation processes, which are vital for understanding carbohydrate chemistry and biochemistry.
  • Pharmaceutical Development: It is used in the synthesis of glycosides that have potential therapeutic applications, particularly in drug design targeting specific biological pathways.
  • Biological Assays: Researchers employ this compound in assays to evaluate enzyme activity, especially in studies related to glycoside hydrolases, enhancing our understanding of metabolic pathways.
  • Natural Product Research: It aids in the extraction and characterization of natural products, helping scientists identify and utilize plant-derived compounds with medicinal properties.
  • Analytical Chemistry: This chemical is used as a standard in chromatographic techniques, providing a reliable reference for quantifying similar compounds in complex mixtures.

Citas