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Catalog Number:
32226
CAS Number:
1017587-57-3
Phenyl 3-O-allyl-2,4,6-tri-O-benzyl-1-thio-β-D-galactopyranoside
Purity:
≥ 98% (HPLC)
Synonym(s):
Gal[246Bn,3All]-β-SPh
Documents
$141.41 /100MG
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Product Information

Phenyl 3-O-allyl-2,4,6-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 serves as a valuable intermediate in the synthesis of complex carbohydrates and can be utilized in the development of glycosylated drugs, enhancing their bioavailability and therapeutic efficacy. Its structural features, including multiple benzyl groups and an allyl substituent, contribute to its stability and reactivity, making it an excellent candidate for further chemical modifications.

In research, this compound can be employed in the study of carbohydrate-protein interactions, providing insights into glycoprotein functions and their roles in biological processes. Additionally, its thio-galactopyranoside structure allows for potential applications in the design of targeted drug delivery systems. By leveraging its unique chemical properties, researchers can explore innovative solutions in drug formulation and development, paving the way for advancements in therapeutic strategies.

Synonyms
Gal[246Bn,3All]-β-SPh
CAS Number
1017587-57-3
Purity
≥ 98% (HPLC)
Molecular Formula
C36H38O5S
Molecular Weight
582.76
MDL Number
MFCD11112183
PubChem ID
76030757
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= -11 to -14° (C=1 in CHCl3
Conditions
Store at 2-8 °C
General Information
Synonyms
Gal[246Bn,3All]-β-SPh
CAS Number
1017587-57-3
Purity
≥ 98% (HPLC)
Molecular Formula
C36H38O5S
Molecular Weight
582.76
MDL Number
MFCD11112183
PubChem ID
76030757
Appearance
White to off-white crystalline powder
Optical Rotation
[a]20/D= -11 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 3-O-allyl-2,4,6-tri-O-benzyl-1-thio-b-D-galactopyranoside is widely utilized in research focused on:

  • Glycosylation Reactions: This compound serves as a valuable glycosyl donor in synthetic organic chemistry, facilitating the formation of glycosidic bonds in complex carbohydrate synthesis.
  • Drug Development: It plays a role in the development of glycosylated drugs, which can enhance the pharmacokinetic properties of therapeutic agents, making them more effective in treating diseases.
  • Biotechnology: Used in the production of glycoproteins, this compound aids in the development of biopharmaceuticals, contributing to advancements in vaccine and antibody production.
  • Research on Carbohydrate Biology: It is instrumental in studying carbohydrate-protein interactions, providing insights into biological processes such as cell signaling and immune responses.
  • Material Science: This chemical is explored for its potential in creating novel materials with specific properties, such as enhanced biocompatibility for medical devices.

Citations