3-(benzyloxy)-4-hydroxybenzoic acid

95%

Reagent Code: #150797
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CAS Number 159832-34-5

science Other reagents with same CAS 159832-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.24 g/mol
Formula C₁₄H₁₂O₄
badge Registry Numbers
MDL Number MFCD23110928
thermostat Physical Properties
Boiling Point 455.2±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.319±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain anti-inflammatory and analgesic agents. It serves as a building block in organic reactions where selective protection of phenolic hydroxyl groups is required, due to the presence of the benzyl-protected hydroxy functionality. Its carboxylic acid group allows for easy derivatization into esters, amides, or other functional groups, making it valuable in medicinal chemistry for constructing complex molecules. Also employed in the development of natural product analogs and in structure-activity relationship (SAR) studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,450.00
inventory 250mg
10-20 days ฿20,520.00
inventory 1g
10-20 days ฿41,040.00

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3-(benzyloxy)-4-hydroxybenzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain anti-inflammatory and analgesic agents. It serves as a building block in organic reactions where selective protection of phenolic hydroxyl groups is required, due to the presence of the benzyl-protected hydroxy functionality. Its carboxylic acid group allows for easy derivatization into esters, amides, or other functional groups, making it valuable in medicinal chemistry for constructing complex molecul

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain anti-inflammatory and analgesic agents. It serves as a building block in organic reactions where selective protection of phenolic hydroxyl groups is required, due to the presence of the benzyl-protected hydroxy functionality. Its carboxylic acid group allows for easy derivatization into esters, amides, or other functional groups, making it valuable in medicinal chemistry for constructing complex molecules. Also employed in the development of natural product analogs and in structure-activity relationship (SAR) studies.

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