tert-Butyl 3-formyl-4-hydroxybenzoate

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Reagent Code: #145413
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CAS Number 1224157-88-3

science Other reagents with same CAS 1224157-88-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.24 g/mol
Formula C₁₂H₁₄O₄
thermostat Physical Properties
Boiling Point 327.1±27.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of anticoagulant drugs such as warfarin and related coumarin derivatives. Its aldehyde and phenolic hydroxyl functional groups allow for selective chemical modifications, enabling the construction of complex aromatic structures. Commonly employed in organic synthesis for introducing the 4-hydroxybenzaldehyde moiety in a protected form, facilitating multi-step reactions where functional group compatibility is crucial. Also utilized in the development of agrochemicals and fine chemicals due to its stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,100.00
inventory 100mg
10-20 days ฿5,070.00

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tert-Butyl 3-formyl-4-hydroxybenzoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of anticoagulant drugs such as warfarin and related coumarin derivatives. Its aldehyde and phenolic hydroxyl functional groups allow for selective chemical modifications, enabling the construction of complex aromatic structures. Commonly employed in organic synthesis for introducing the 4-hydroxybenzaldehyde moiety in a protected form, facilitating multi-step reactions where functional group compatibility is cr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of anticoagulant drugs such as warfarin and related coumarin derivatives. Its aldehyde and phenolic hydroxyl functional groups allow for selective chemical modifications, enabling the construction of complex aromatic structures. Commonly employed in organic synthesis for introducing the 4-hydroxybenzaldehyde moiety in a protected form, facilitating multi-step reactions where functional group compatibility is crucial. Also utilized in the development of agrochemicals and fine chemicals due to its stability and reactivity profile.

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