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Catalog Number:
32111
CAS Number:
183875-28-7
Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside
Purity:
≥ 98% (HPLC)
Synonym(s):
Gal[2Ac,346Bn]-β-SPh
Documents
$93.14 /100MG
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Product Information

Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside is a specialized glycoside that exhibits unique properties beneficial for various applications in the fields of biochemistry and pharmaceuticals. This compound is recognized for its ability to serve as a versatile building block in the synthesis of complex carbohydrates and glycoproteins, which are essential in drug development and biological research. Its structural features, including the thio-galactopyranoside moiety, enhance its stability and reactivity, making it an ideal candidate for studies involving enzyme interactions and carbohydrate recognition processes.

Researchers and industry professionals can leverage this compound in the development of targeted drug delivery systems and in the exploration of carbohydrate-based therapeutics. Its acetyl and benzyl groups contribute to its solubility and compatibility with various solvents, facilitating its use in diverse experimental setups. Additionally, the compound's unique structure may provide advantages over similar glycosides, particularly in enhancing bioavailability and specificity in biological applications. Overall, Phenyl 2-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside stands out as a valuable tool for advancing research and innovation in glycoscience.

Synonyms
Gal[2Ac,346Bn]-β-SPh
CAS Number
183875-28-7
Purity
≥ 98% (HPLC)
Molecular Formula
C35H36O6S
Molecular Weight
584.73
MDL Number
MFCD27976837
PubChem ID
14444925
Melting Point
111? C
Optical Rotation
[a]20/D= +10 to +14° (C=1 in CHCL3
Conditions
Store at 2-8 °C
General Information
Synonyms
Gal[2Ac,346Bn]-β-SPh
CAS Number
183875-28-7
Purity
≥ 98% (HPLC)
Molecular Formula
C35H36O6S
Molecular Weight
584.73
MDL Number
MFCD27976837
PubChem ID
14444925
Melting Point
111? C
Optical Rotation
[a]20/D= +10 to +14° (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-O-acetyl-3,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a glycosyl donor in synthetic organic chemistry, facilitating the formation of glycosidic bonds in the development of complex carbohydrates.
  • Drug Development: Its structural properties make it valuable in pharmaceutical research, particularly in the design of glycosylated drugs that can enhance bioavailability and target specificity.
  • Biotechnology: Used in the production of glycoproteins, this compound aids in the study of protein interactions and functions, which are crucial for understanding biological processes.
  • Diagnostic Applications: It can be employed in the development of diagnostic tools, such as assays that detect specific biomolecules, improving accuracy in medical testing.
  • Research on Carbohydrate Chemistry: This compound is instrumental in exploring carbohydrate structures and their roles in biological systems, contributing to advancements in fields like immunology and cell biology.

Citations