Methyl3-bromo-5-(((tert-butyldiphenylsilyl)oxy)methyl)benzoate

98%

Reagent Code: #213523
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CAS Number 2411829-04-2

science Other reagents with same CAS 2411829-04-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 483.47 g/mol
Formula C₂₅H₂₇BrO₃Si
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the construction of complex molecules such as natural products and pharmaceuticals. Its functional groups—ester and silyl-protected hydroxymethyl—allow selective transformations, enabling stepwise elaboration of molecular architecture. The bromo substituent serves as a handle for cross-coupling reactions, such as Suzuki or Heck reactions, facilitating carbon–carbon bond formation. The silyl ether group provides stability to the alcohol functionality under various reaction conditions and can be removed selectively when needed, making this compound valuable in multi-step synthetic sequences, especially in medicinal chemistry and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,880.00
Methyl3-bromo-5-(((tert-butyldiphenylsilyl)oxy)methyl)benzoate
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Used as a key intermediate in organic synthesis, particularly in the construction of complex molecules such as natural products and pharmaceuticals. Its functional groups—ester and silyl-protected hydroxymethyl—allow selective transformations, enabling stepwise elaboration of molecular architecture. The bromo substituent serves as a handle for cross-coupling reactions, such as Suzuki or Heck reactions, facilitating carbon–carbon bond formation. The silyl ether group provides stability to the alcohol func

Used as a key intermediate in organic synthesis, particularly in the construction of complex molecules such as natural products and pharmaceuticals. Its functional groups—ester and silyl-protected hydroxymethyl—allow selective transformations, enabling stepwise elaboration of molecular architecture. The bromo substituent serves as a handle for cross-coupling reactions, such as Suzuki or Heck reactions, facilitating carbon–carbon bond formation. The silyl ether group provides stability to the alcohol functionality under various reaction conditions and can be removed selectively when needed, making this compound valuable in multi-step synthetic sequences, especially in medicinal chemistry and materials science.

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