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Catalog Number:
21352
CAS Number:
157843-41-9
2-Cloro-4-nitrofenil-aL-fucopiranósido
Purity:
≥ 99 % (HPLC)
Synonym(s):
2-Cloro-4-nitrofenil-6-desoxi-aL-galactopiranósido
Documents
$58.39 /100 mg
Tamaño
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Product Information

2-Chloro-4-nitrophenyl-α-L-fucopyranoside is a specialized glycoside that serves as a valuable tool in biochemical research and applications. This compound is recognized for its unique structural features, which include a chloro and nitro substituent on the phenyl ring, enhancing its reactivity and utility in various chemical reactions. Researchers often utilize this compound in the synthesis of glycosylated derivatives, which are crucial for studying carbohydrate-protein interactions and enzyme activities. Its ability to act as a substrate for specific glycosidases makes it particularly relevant in enzymology and carbohydrate chemistry.

In addition to its research applications, 2-Chloro-4-nitrophenyl-α-L-fucopyranoside is also employed in the development of diagnostic assays and therapeutic agents. The compound's distinctive properties allow for the exploration of fucose-related biological processes, making it a significant player in the study of glycosylation patterns in cells. Its versatility and effectiveness in various applications underscore its importance in both academic and industrial settings, providing researchers with a reliable tool for advancing their work in glycoscience.

Synonyms
2-Cloro-4-nitrofenil-6-desoxi-aL-galactopiranósido
CAS Number
157843-41-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H14ClNO7
Molecular Weight
319.8
MDL Number
MFCD04972056
PubChem ID
4525307
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
2-Cloro-4-nitrofenil-6-desoxi-aL-galactopiranósido
CAS Number
157843-41-9
Purity
≥ 99 % (HPLC)
Molecular Formula
C12H14ClNO7
Molecular Weight
319.8
MDL Number
MFCD04972056
PubChem ID
4525307
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloro-4-nitrophenyl-a-L-fucopyranoside is widely utilized in research focused on:

  • Glycobiology Research: This compound serves as a valuable substrate for studying glycosylation processes, helping researchers understand carbohydrate structures and their biological functions.
  • Enzyme Assays: It is commonly used in enzyme assays to measure the activity of fucosidases, which are important in various biological pathways and disease mechanisms.
  • Drug Development: The compound can be employed in the development of new therapeutics targeting glycan-related diseases, offering potential advantages in specificity and efficacy over traditional compounds.
  • Diagnostic Tools: It is utilized in the creation of diagnostic assays for detecting specific glycan markers in diseases, aiding in early diagnosis and personalized medicine approaches.
  • Biotechnology Applications: This chemical plays a role in biotechnological processes, such as the production of glycoproteins, enhancing the yield and quality of biopharmaceuticals.

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