(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 |
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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 |
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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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