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

99.5%

Reagent Code: #141925
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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 nucleoside analogs. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. Commonly employed in the production of protease inhibitors and other bioactive molecules where controlled functionalization of aromatic rings is required. Also utilized in research settings for modifying solubility and stability of complex molecules during synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,880.00
250mg
10-20 days ฿4,580.00
1g
10-20 days ฿9,830.00
5g
10-20 days ฿46,690.00
25g
10-20 days ฿170,820.00

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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 nucleoside analogs. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. Commonly employed in the production of protease inhibitors and other bioactive molecules where controlled functionalization of aromatic rings is required. Also utilized in research settings for modifying solubility and stability of complex mole

Used as a key intermediate in the synthesis of antiviral drugs, particularly in the preparation of nucleoside analogs. Its silyl-protected hydroxyl groups allow selective reactivity in multi-step organic syntheses, making it valuable in pharmaceutical development. Commonly employed in the production of protease inhibitors and other bioactive molecules where controlled functionalization of aromatic rings is required. Also utilized in research settings for modifying solubility and stability of complex molecules during synthesis.

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