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Catalog Number:
32287
CAS Number:
197005-22-4
Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-ॆ-D-glucopyranoside
Purity:
≥ 99% (HPLC)
Documents
$100.05 /25MG
Pack Size Availability Price
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Product Information

Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-b-D-glucopyranoside is a versatile compound that plays a significant role in the field of organic synthesis and carbohydrate chemistry. This compound, characterized by its unique thio-glycoside structure, is particularly valuable for researchers focusing on glycosylation reactions and the development of glycoside derivatives. Its acetyl groups enhance solubility and stability, making it an ideal candidate for various applications, including the synthesis of complex carbohydrates and bioactive molecules.

In the pharmaceutical industry, this compound can be utilized to create novel drug candidates with improved bioavailability and efficacy. Additionally, its ability to serve as a building block in the synthesis of glycoproteins and glycolipids opens up new avenues for research in biochemistry and molecular biology. With its unique properties and potential applications, Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-b-D-glucopyranoside stands out as a valuable tool for scientists and industry professionals alike, facilitating advancements in drug development and biochemical research.

CAS Number
197005-22-4
Purity
≥ 99% (HPLC)
Molecular Formula
C21H26O8S
Molecular Weight
438.49
MDL Number
MFCD11112185
PubChem ID
75059434
Melting Point
113 - 117 °C
Appearance
White to almost white powder to crystal
Conditions
Store at 2 - 8 °C
General Information
CAS Number
197005-22-4
Purity
≥ 99% (HPLC)
Molecular Formula
C21H26O8S
Molecular Weight
438.49
MDL Number
MFCD11112185
PubChem ID
75059434
Melting Point
113 - 117 °C
Appearance
White to almost white powder to crystal
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-b-D-glucopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in synthetic chemistry, facilitating the formation of glycosidic bonds, which are crucial in creating complex carbohydrates.
  • Drug Development: Its unique structure allows researchers to explore new drug candidates, particularly in the development of glycosylated pharmaceuticals that can enhance bioavailability and efficacy.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, improving the functionality of diagnostic tools and therapeutic agents.
  • Research in Carbohydrate Chemistry: The compound is pivotal in studies aimed at understanding carbohydrate interactions and their biological roles, aiding in the exploration of new therapeutic targets.
  • Food Industry Applications: Its derivatives can be used in flavoring and preservation, enhancing the sensory properties of food products while maintaining safety and stability.

Citations