4-(tert-Butoxymethyl)benzoic acid

95%

Reagent Code: #129204
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CAS Number 34224-31-2

science Other reagents with same CAS 34224-31-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.25 g/mol
Formula C₁₂H₁₆O₃
badge Registry Numbers
MDL Number MFCD01862971
thermostat Physical Properties
Melting Point 147-151 °C
Boiling Point 313.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.091±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its carboxylic acid group allows for easy amide or ester formation, making it valuable in drug development. The tert-butoxymethyl protecting group enhances solubility and stability during multi-step syntheses, and can be selectively removed under mild acidic conditions. Commonly employed in the preparation of bioactive compounds and functionalized aromatic systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,600.00
inventory 1g
10-20 days ฿19,200.00
inventory 5g
10-20 days ฿57,600.00

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4-(tert-Butoxymethyl)benzoic acid
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its carboxylic acid group allows for easy amide or ester formation, making it valuable in drug development. The tert-butoxymethyl protecting group enhances solubility and stability during multi-step syntheses, and can be selectively removed under mild acidic conditions. Commonly employed in the preparation of bioactive compounds and functionalized aromatic systems.

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for constructing complex molecules. Its carboxylic acid group allows for easy amide or ester formation, making it valuable in drug development. The tert-butoxymethyl protecting group enhances solubility and stability during multi-step syntheses, and can be selectively removed under mild acidic conditions. Commonly employed in the preparation of bioactive compounds and functionalized aromatic systems.

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