3-[(2-Tetrahydropyranyl)oxy]propanoic Acid

≥95%

Reagent Code: #244753
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CAS Number 1221443-23-7

science Other reagents with same CAS 1221443-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.19 g/mol
Formula C₈H₁₄O₄
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MDL Number MFCD11554187
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry, Lightproof, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its protected alcohol functionality makes it valuable in multi-step synthesis where selective reactions are required. The tetrahydropyranyl group acts as a protecting group for alcohols, allowing controlled deprotection under mild acidic conditions. This compound is also utilized in the preparation of biologically active molecules, including drug candidates that require functionalized carboxylic acid derivatives. Its stability and reactivity profile make it suitable for use in peptide modifications and prodrug design.

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inventory 1g
10-20 days ฿17,800.00

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3-[(2-Tetrahydropyranyl)oxy]propanoic Acid
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its protected alcohol functionality makes it valuable in multi-step synthesis where selective reactions are required. The tetrahydropyranyl group acts as a protecting group for alcohols, allowing controlled deprotection under mild acidic conditions. This compound is also utilized in the preparation of biologically active molecules, including drug candidates that require functionalized carboxylic a

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical manufacturing. Its protected alcohol functionality makes it valuable in multi-step synthesis where selective reactions are required. The tetrahydropyranyl group acts as a protecting group for alcohols, allowing controlled deprotection under mild acidic conditions. This compound is also utilized in the preparation of biologically active molecules, including drug candidates that require functionalized carboxylic acid derivatives. Its stability and reactivity profile make it suitable for use in peptide modifications and prodrug design.

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