(R)-3-((tert-butyldiphenylsilyl)oxy)propane-1,2-diol

95%

  • Product Code: 84821
  CAS:    125111-27-5
Molecular Weight: 330.49 g./mol Molecular Formula: C₁₉H₂₆O₃Si
EC Number: MDL Number: MFCD30537266
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used in organic synthesis as a protecting group for hydroxyl functions in complex molecular constructions. Its structure, featuring a tert-butyldiphenylsilyl group, makes it particularly useful in the selective protection of diols during multi-step synthetic processes, especially in the synthesis of pharmaceuticals and fine chemicals. The compound is often employed in the preparation of chiral intermediates, where the protection and subsequent deprotection of hydroxyl groups are crucial for achieving the desired stereochemistry. Additionally, it finds application in the synthesis of natural products and bioactive molecules, where precise control over the reactivity of functional groups is essential. Its stability under various reaction conditions allows for its use in a wide range of synthetic transformations, including those involving nucleophiles and electrophiles.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿3,042.00
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0.250 10-20 days ฿5,850.00
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1.000 10-20 days ฿11,700.00
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(R)-3-((tert-butyldiphenylsilyl)oxy)propane-1,2-diol
This chemical is primarily used in organic synthesis as a protecting group for hydroxyl functions in complex molecular constructions. Its structure, featuring a tert-butyldiphenylsilyl group, makes it particularly useful in the selective protection of diols during multi-step synthetic processes, especially in the synthesis of pharmaceuticals and fine chemicals. The compound is often employed in the preparation of chiral intermediates, where the protection and subsequent deprotection of hydroxyl groups are crucial for achieving the desired stereochemistry. Additionally, it finds application in the synthesis of natural products and bioactive molecules, where precise control over the reactivity of functional groups is essential. Its stability under various reaction conditions allows for its use in a wide range of synthetic transformations, including those involving nucleophiles and electrophiles.
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