N-(TERT-BUTOXYCARBONYL)-D-GLUCOSAMINE

97%

  • Product Code: 98051
  CAS:    75251-80-8
Molecular Weight: 279.29 g./mol Molecular Formula: C₁₁H₂₁NO₇
EC Number: MDL Number: MFCD00134540
Melting Point: 194 °C (dec.) (lit.) Boiling Point: 550.7±50.0 °C(Predicted)
Density: 1.321±0.06 g/cm3(Predicted) Storage Condition: room temperature
Product Description: N-(Tert-butoxycarbonyl)-D-glucosamine is widely used in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in carbohydrate chemistry research. It serves as a protected form of glucosamine, enabling selective reactions in the development of oligosaccharides and glycoproteins. This compound is particularly valuable in the preparation of glycosyl donors and acceptors, facilitating the study of glycosylation processes. Additionally, it is utilized in the production of bioactive molecules, including potential drug candidates targeting inflammation, cancer, and microbial infections. Its protective group ensures stability during chemical transformations, making it a key intermediate in organic and medicinal chemistry applications.
Product Specification:
Test Specification
APPEARANCE WHITE POWDER OR CRYSTALS
PURITY 96.5-100
CARBON 45.6-49.0
NitrogenN 4.8- 5.2%
OPTICAL ROTATION 63-2DEGREES (C=1%, METHANOL)
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿2,950.00
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N-(TERT-BUTOXYCARBONYL)-D-GLUCOSAMINE
N-(Tert-butoxycarbonyl)-D-glucosamine is widely used in the synthesis of complex carbohydrates and glycoconjugates, playing a crucial role in carbohydrate chemistry research. It serves as a protected form of glucosamine, enabling selective reactions in the development of oligosaccharides and glycoproteins. This compound is particularly valuable in the preparation of glycosyl donors and acceptors, facilitating the study of glycosylation processes. Additionally, it is utilized in the production of bioactive molecules, including potential drug candidates targeting inflammation, cancer, and microbial infections. Its protective group ensures stability during chemical transformations, making it a key intermediate in organic and medicinal chemistry applications.
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