• Fmoc-Thr[GalNAc(Ac)3-alpha-D]-OH (CAS 116783-35-8) - TCI F1368 - AMI Scientific
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TCI

CAS 116783-35-8

Fmoc-Thr[GalNAc(Ac)3-alpha-D]-OH TCI F1368

Fmoc-Thr[GalNAc(Ac)3-alpha-D]-OH TCI F1368
Rp 6.463.800,00
Rp 6.463.800,00
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TCI F1368 116783-35-8 Fmoc-Thr[GalNAc(Ac)3-alpha-D]-OH is a specialized chemical compound used in chemical biology and glycoscience research. This compound serves as a key reagent in the synthesis of complex molecules, particularly in the development of pharmaceuticals and biomedical applications. It is a Fmoc-protected derivative of threonine linked to a modified GalNAc (GalNAc(Ac)3-alpha-D) moiety, making it highly relevant for advanced chemical synthesis. Its unique structure enables it to participate in precise chemical reactions under controlled laboratory conditions.

The compound's chemical structure and functional groups make it a preferred choice for researchers working in glycoscience. The Fmoc protecting group facilitates deprotection during molecular synthesis, allowing for controlled and selective reactions. Its ability to interact with specific functional groups, such as amines and hydroxyls, enhances its utility in substitution and conjugation reactions. These properties make it an essential tool for creating bioactive molecules with specific biological functions.

In Indonesian laboratories, this compound is widely used in studies related to glycoscience and the development of bioactive compounds. Research institutions and universities rely on it for molecular interaction studies and the advancement of glycosidic-based therapies. Its application supports both fundamental and applied research in the field of chemical biology.

  • Glycoscience Research: This compound is ideal for studying glycosylation processes and carbohydrate-based molecular interactions due to its specific structural features.
  • Pharmaceutical Development: It is used in the synthesis of complex molecules, particularly in drug development, where precise chemical modifications are required.
  • Bioconjugation Studies: The presence of reactive functional groups allows it to be used in conjugation reactions, making it suitable for creating targeted therapeutic agents.
  • Molecular Synthesis: Its Fmoc group enables controlled deprotection, making it a valuable reagent in the synthesis of bioactive compounds.
  • Biomedical Research: It supports research into glycosidic-based therapies and molecular interactions relevant to disease mechanisms.

Brand TCI
CAS number 116783-35-8
Molecular formula —
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Category Chemistry > Chemical Biology > Glycoscience
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Storage Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption, which could affect its chemical stability. Due to its chemical complexity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation should be maintained in the workspace to minimize exposure to vapors. The compound is not typically hazardous in normal handling conditions, but standard laboratory safety protocols should be followed to ensure safe usage and storage.

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