(S)-(1-tosylaziridin-2-yl)methanol

95%

  • Product Code: 84858
  CAS:    167029-54-1
Molecular Weight: 227.28 g./mol Molecular Formula: C₁₀H₁₃NO₃S
EC Number: MDL Number: MFCD31802245
Melting Point: Boiling Point: 391.3±44.0 °C(Predicted)
Density: 1.365±0.06 g/cm3(Predicted) Storage Condition: room temperature
Product Description: This chemical is primarily utilized in the synthesis of chiral compounds, particularly in the development of pharmaceuticals and bioactive molecules. Its aziridine ring structure makes it a valuable intermediate in organic synthesis, enabling the formation of complex molecules with high stereochemical control. It is often employed in the preparation of beta-amino alcohols, which are important building blocks for drugs targeting cardiovascular diseases, infections, and neurological disorders. Additionally, it finds use in asymmetric synthesis, where its chiral center aids in creating enantiomerically pure compounds, essential for producing effective and safe medications. Its role in medicinal chemistry highlights its significance in advancing drug discovery and development.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $291.53
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0.250 10-20 days $583.07
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1.000 10-20 days $1,166.13
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(S)-(1-tosylaziridin-2-yl)methanol
This chemical is primarily utilized in the synthesis of chiral compounds, particularly in the development of pharmaceuticals and bioactive molecules. Its aziridine ring structure makes it a valuable intermediate in organic synthesis, enabling the formation of complex molecules with high stereochemical control. It is often employed in the preparation of beta-amino alcohols, which are important building blocks for drugs targeting cardiovascular diseases, infections, and neurological disorders. Additionally, it finds use in asymmetric synthesis, where its chiral center aids in creating enantiomerically pure compounds, essential for producing effective and safe medications. Its role in medicinal chemistry highlights its significance in advancing drug discovery and development.
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