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Catalog Number:
42336
CAS Number:
1820572-28-8
Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-β-D-galactopyranoside
Purity:
≥ 98% (HPLC)
Synonym(s):
Gal[246Ac,3All]-β-SPh
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Product Information

Phenyl 2,4,6-tri-O-acetyl-3-O-allyl-1-thio-b-D-galactopyranoside is a specialized glycoside derivative that exhibits unique properties beneficial for various applications in the fields of biochemistry and pharmaceuticals. This compound is characterized by its acetylated galactopyranoside structure, which enhances its stability and solubility, making it an ideal candidate for use in drug formulation and delivery systems. Its thioether functionality provides additional reactivity, allowing for potential modifications that can lead to the development of novel therapeutic agents.

Researchers and industry professionals can leverage this compound in the synthesis of glycosylated drugs, where it can serve as a building block for more complex molecules. Its ability to participate in glycosylation reactions opens avenues for creating targeted drug delivery systems, particularly in cancer therapy and other diseases where precision medicine is crucial. Moreover, its unique structural features may offer advantages over similar compounds, such as improved bioavailability and reduced side effects, making it a valuable addition to any research or development project focused on innovative pharmaceutical solutions.

Synonyms
Gal[246Ac,3All]-β-SPh
CAS Number
1820572-28-8
Purity
≥ 98% (HPLC)
Molecular Formula
C21H26O8S
Molecular Weight
438.49
PubChem ID
75059434
Appearance
White to off-white powder
Optical Rotation
a20D = 27 - 30 ° (C=1 in CHCl3)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Gal[246Ac,3All]-β-SPh
CAS Number
1820572-28-8
Purity
≥ 98% (HPLC)
Molecular Formula
C21H26O8S
Molecular Weight
438.49
PubChem ID
75059434
Appearance
White to off-white powder
Optical Rotation
a20D = 27 - 30 ° (C=1 in CHCl3)
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-galactopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in organic synthesis, facilitating the formation of glycosidic bonds. This is particularly useful in the development of complex carbohydrates for pharmaceuticals.
  • Drug Development: Its unique structure allows for modifications that can enhance the bioavailability and efficacy of drugs, making it valuable in the pharmaceutical industry for creating new therapeutic agents.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostic applications.
  • Research in Carbohydrate Chemistry: It is a key reagent in the study of carbohydrate chemistry, aiding researchers in understanding glycan structures and their biological roles, which can lead to advancements in vaccine development.
  • Food Industry Applications: The compound can be explored for use in food science, particularly in flavoring and preservation, leveraging its chemical properties to enhance food products.

Citations