1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose

98%

  • Product Code: 98140
  Alias:    1,2,3,5-tetra-oxo-acetyl-D-ribofuranose, β-D-ribofuranose 1,2,3,5-tetraacetate
  CAS:    13035-61-5
Molecular Weight: 318.28 g./mol Molecular Formula: C₁₃H₁₈O₉
EC Number: 235-898-5 MDL Number: MFCD00005358
Melting Point: 81-83 °C(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: This chemical is primarily used as an intermediate in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It plays a key role in the production of modified ribose sugars, which are essential components in the creation of nucleotide-based therapeutics. Additionally, it is employed in the preparation of prodrugs, enhancing the bioavailability and stability of active pharmaceutical ingredients. Its acetyl groups protect the ribose moiety during chemical reactions, ensuring precise modifications in the synthesis process. This compound is also utilized in research settings for studying carbohydrate chemistry and developing novel drug delivery systems.
Product Specification:
Test Specification
APPEARANCE white crystals or powder or crystalline powder
PURITY 97.5-100
SPECIFIC ROTATION A20DC5 MEOH -16.0
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿250.00
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-
25.000 10-20 days ฿460.00
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100.000 10-20 days ฿680.00
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-
500.000 10-20 days ฿1,860.00
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-
2500.000 10-20 days ฿7,680.00
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1,2,3,5-Tetra-O-acetyl-β-D-ribofuranose
This chemical is primarily used as an intermediate in the synthesis of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. It plays a key role in the production of modified ribose sugars, which are essential components in the creation of nucleotide-based therapeutics. Additionally, it is employed in the preparation of prodrugs, enhancing the bioavailability and stability of active pharmaceutical ingredients. Its acetyl groups protect the ribose moiety during chemical reactions, ensuring precise modifications in the synthesis process. This compound is also utilized in research settings for studying carbohydrate chemistry and developing novel drug delivery systems.
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