tert-butyl-dimethyl-(1,3-thiazol-4-ylmethoxy)silane

95%

Reagent Code: #238965
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CAS Number 875548-61-1

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.42 g/mol
Formula C₁₀H₁₉NOSSi
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is the tert-butyldimethylsilyl (TBDMS) ether of (1,3-thiazol-4-yl)methanol, serving as a protected building block in organic synthesis. The silyl protecting group shields the hydroxyl functionality, providing stability under basic conditions and selective deprotection with fluoride ions (e.g., TBAF) or mild acids. Its thiazole moiety enhances solubility in organic solvents and compatibility with diverse reaction conditions, making it valuable for multi-step assemblies in pharmaceutical API development, agrochemicals, and fine chemicals where precise manipulation of heterocyclic intermediates is essential.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿28,500.00
tert-butyl-dimethyl-(1,3-thiazol-4-ylmethoxy)silane
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This compound is the tert-butyldimethylsilyl (TBDMS) ether of (1,3-thiazol-4-yl)methanol, serving as a protected building block in organic synthesis. The silyl protecting group shields the hydroxyl functionality, providing stability under basic conditions and selective deprotection with fluoride ions (e.g., TBAF) or mild acids. Its thiazole moiety enhances solubility in organic solvents and compatibility with diverse reaction conditions, making it valuable for multi-step assemblies in pharmaceutical API dev
This compound is the tert-butyldimethylsilyl (TBDMS) ether of (1,3-thiazol-4-yl)methanol, serving as a protected building block in organic synthesis. The silyl protecting group shields the hydroxyl functionality, providing stability under basic conditions and selective deprotection with fluoride ions (e.g., TBAF) or mild acids. Its thiazole moiety enhances solubility in organic solvents and compatibility with diverse reaction conditions, making it valuable for multi-step assemblies in pharmaceutical API development, agrochemicals, and fine chemicals where precise manipulation of heterocyclic intermediates is essential.
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