3,4-bis((tert-butyldimethylsilyl)oxy)benzoic acid

98%

Reagent Code: #141926
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CAS Number 154083-18-8

science Other reagents with same CAS 154083-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 382.64 g/mol
Formula C₁₉H₃₄O₄Si₂
thermostat Physical Properties
Boiling Point 395.0±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.989±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of HIV protease inhibitors. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. The carboxylic acid functionality enables coupling reactions, facilitating the construction of complex molecular architectures. Commonly employed in medicinal chemistry for modifying solubility and bioavailability during drug design.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,890.00
inventory 250mg
10-20 days ฿3,050.00
inventory 1g
10-20 days ฿6,560.00
inventory 5g
10-20 days ฿31,130.00
inventory 25g
10-20 days ฿125,990.00

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3,4-bis((tert-butyldimethylsilyl)oxy)benzoic acid
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Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of HIV protease inhibitors. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. The carboxylic acid functionality enables coupling reactions, facilitating the construction of complex molecular architectures. Commonly employed in medicinal chemistry for modifying solubility and bioavailability during drug design.

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of HIV protease inhibitors. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. The carboxylic acid functionality enables coupling reactions, facilitating the construction of complex molecular architectures. Commonly employed in medicinal chemistry for modifying solubility and bioavailability during drug design.

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