2-Deoxy-L-ribose

99%

  • Product Code: 97159
  Alias:    2-Deoxy-L-ribose
  CAS:    18546-37-7
Molecular Weight: 134.13 g./mol Molecular Formula: C₅H₁₀O₄
EC Number: MDL Number: MFCD00132941
Melting Point: 69-72°C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used primarily in biochemical research, 2-Deoxy-L-ribose plays a crucial role in the synthesis of nucleosides and nucleotides, which are fundamental components of DNA. It is also employed in the study of metabolic pathways, particularly those involving carbohydrate metabolism. Additionally, this compound is utilized in the development of antiviral and anticancer drugs, where it serves as a building block for modified nucleosides that can inhibit the replication of viruses or cancer cells. In the field of organic chemistry, it is used as a chiral starting material for the synthesis of complex molecules, aiding in the exploration of stereochemical reactions and enzyme mechanisms.
Product Specification:
Test Specification
CARBON BY ELEMENTAL ANALYSIS 43.9-44.8
HYDROGEN BY ELEMENTAL ANALYSIS 7.3-7.5
IGNITION RESIDUE AS SULFATE 0-1
PURITYHPLC 99-100
H2O24HRS 52-57
WATER BY KARL FISCHER 0-1
APPEARANCE White or off-white powder
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿560.00
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1.000 10-20 days ฿1,780.00
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-
5.000 10-20 days ฿7,620.00
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2-Deoxy-L-ribose
Used primarily in biochemical research, 2-Deoxy-L-ribose plays a crucial role in the synthesis of nucleosides and nucleotides, which are fundamental components of DNA. It is also employed in the study of metabolic pathways, particularly those involving carbohydrate metabolism. Additionally, this compound is utilized in the development of antiviral and anticancer drugs, where it serves as a building block for modified nucleosides that can inhibit the replication of viruses or cancer cells. In the field of organic chemistry, it is used as a chiral starting material for the synthesis of complex molecules, aiding in the exploration of stereochemical reactions and enzyme mechanisms.
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