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Catalog Number:
32254
CAS Number:
36875-26-0
N-Trifluoroacetyl-D-glucosamine
Purity:
≥ 96% (T)
Documents
$93.14 /100MG
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Product Information

N-Trifluoroacetyl-D-glucosamine is a versatile compound known for its unique trifluoroacetyl group, which enhances its reactivity and solubility in various solvents. This chemical is particularly valuable in the fields of medicinal chemistry and biochemistry, where it serves as a crucial building block for the synthesis of glycosylated compounds and derivatives. Its ability to modify carbohydrate structures makes it an essential tool in the development of pharmaceuticals, particularly in the design of glycosylated drugs that can improve bioavailability and efficacy. Researchers have utilized N-Trifluoroacetyl-D-glucosamine in the synthesis of glycopeptides and other biologically active molecules, showcasing its importance in drug discovery and development.

Moreover, this compound's unique properties allow for selective reactions that can lead to the formation of complex molecular architectures, making it a preferred choice for chemists looking to innovate in carbohydrate chemistry. Its application extends to the study of glycoproteins and their interactions, providing insights that are critical in understanding various biological processes. With its broad range of applications and significant advantages in synthetic pathways, N-Trifluoroacetyl-D-glucosamine stands out as a key reagent for researchers and industry professionals alike.

CAS Number
36875-26-0
Purity
≥ 96% (T)
Molecular Formula
C8H12F3NO6
Molecular Weight
275.18
MDL Number
MFCD00059807
Appearance
White to light reddish yellow crystaline
Optical Rotation
[a]20/D= +13 to +17° (C=1.5 in H2O)(24hrs allow)
Conditions
Store at RT
General Information
CAS Number
36875-26-0
Purity
≥ 96% (T)
Molecular Formula
C8H12F3NO6
Molecular Weight
275.18
MDL Number
MFCD00059807
Appearance
White to light reddish yellow crystaline
Optical Rotation
[a]20/D= +13 to +17° (C=1.5 in H2O)(24hrs allow)
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

N-Trifluoroacetyl-D-glucosamine is widely utilized in research focused on

  • Drug Development: This compound serves as a crucial intermediate in synthesizing various pharmaceuticals, particularly in the development of anti-inflammatory and anti-cancer drugs.
  • Biochemical Research: It is often used in studies involving glycosylation processes, helping researchers understand carbohydrate interactions in biological systems.
  • Diagnostic Applications: The compound can be employed in the development of diagnostic agents, enhancing the detection of specific biomarkers in medical testing.
  • Food Industry: It finds applications in food science, particularly in the study of carbohydrate metabolism and the development of functional food ingredients.
  • Material Science: N-Trifluoroacetyl-D-glucosamine is explored in creating novel materials with unique properties, such as improved biocompatibility for medical devices.

Citations