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

95%

Reagent Code: #84821
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CAS Number 125111-27-5

blur_circular Chemical Specifications

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Weight 330.49 g/mol
Formula C₁₉H₂₆O₃Si
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MDL Number MFCD30537266
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description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,042.00
inventory 250mg
10-20 days ฿5,850.00
inventory 1g
10-20 days ฿11,700.00
(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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