3-((tert-butyldimethylsilyl)oxy)propyl 4-methylbenzenesulfonate

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Reagent Code: #242906
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CAS Number 115306-83-7

science Other reagents with same CAS 115306-83-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 344.54 g/mol
Formula C₁₆H₂₈O₄SSi
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the protection and activation of hydroxyl groups during complex molecule assembly. Its primary application lies in the pharmaceutical and agrochemical industries, where it enables selective functionalization in multi-step syntheses. The silyl ether group acts as a protecting group for alcohols, while the tosylate moiety serves as a good leaving group, facilitating nucleophilic substitution reactions. This dual functionality makes it valuable for constructing carbon-oxygen and carbon-carbon bonds in sensitive or sterically hindered systems. It is also employed in the synthesis of natural products and bioactive molecules where precise control over reactivity and regioselectivity is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,850.00
inventory 250mg
10-20 days ฿3,090.00
inventory 1g
10-20 days ฿6,180.00

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3-((tert-butyldimethylsilyl)oxy)propyl 4-methylbenzenesulfonate
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Used as a key intermediate in organic synthesis, particularly in the protection and activation of hydroxyl groups during complex molecule assembly. Its primary application lies in the pharmaceutical and agrochemical industries, where it enables selective functionalization in multi-step syntheses. The silyl ether group acts as a protecting group for alcohols, while the tosylate moiety serves as a good leaving group, facilitating nucleophilic substitution reactions. This dual functionality makes it valuabl

Used as a key intermediate in organic synthesis, particularly in the protection and activation of hydroxyl groups during complex molecule assembly. Its primary application lies in the pharmaceutical and agrochemical industries, where it enables selective functionalization in multi-step syntheses. The silyl ether group acts as a protecting group for alcohols, while the tosylate moiety serves as a good leaving group, facilitating nucleophilic substitution reactions. This dual functionality makes it valuable for constructing carbon-oxygen and carbon-carbon bonds in sensitive or sterically hindered systems. It is also employed in the synthesis of natural products and bioactive molecules where precise control over reactivity and regioselectivity is required.

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