(3-Bromopropoxy)-tert-butyldimethylsilane

97%

  • Product Code: 63682
  Alias:    3-Bromopropyl tert-butyl dimethyl siloxane
  CAS:    89031-84-5
Molecular Weight: 253.25 g./mol Molecular Formula: C₉H₂₁BrOSi
EC Number: MDL Number: MFCD00216589
Melting Point: Boiling Point: 182 °C(lit.)
Density: 1.093 g/mL at 25 °C(lit.) Storage Condition: 2~8℃, sealed, protected from light
Product Description: (3-Bromopropoxy)-tert-butyldimethylsilane is commonly used as a versatile reagent in organic synthesis, particularly in the protection and modification of functional groups. It is often employed in the preparation of complex molecules, where it serves as a protecting group for alcohols or hydroxyl-containing compounds. The tert-butyldimethylsilyl (TBDMS) group introduced by this reagent is stable under various reaction conditions, allowing selective transformations in multi-step synthetic pathways. Additionally, the 3-bromopropoxy moiety can act as a linker or spacer in the synthesis of bioactive compounds, enabling further functionalization or conjugation. This chemical is also utilized in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular structure is critical. Its role in facilitating efficient and selective synthetic processes makes it a valuable tool in modern chemical research and industrial applications.
Product Specification:
Test Specification
PurityGC 97-100
REFRACTIVE INDEX N20D 1.45-1.454
SPECIFIC GRAVITY 2020C 1.09-1.095
APPEARANCE COLORLESS LIQUID
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿870.00
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5.000 10-20 days ฿1,000.00
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25.000 10-20 days ฿3,260.00
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100.000 10-20 days ฿10,420.00
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(3-Bromopropoxy)-tert-butyldimethylsilane
(3-Bromopropoxy)-tert-butyldimethylsilane is commonly used as a versatile reagent in organic synthesis, particularly in the protection and modification of functional groups. It is often employed in the preparation of complex molecules, where it serves as a protecting group for alcohols or hydroxyl-containing compounds. The tert-butyldimethylsilyl (TBDMS) group introduced by this reagent is stable under various reaction conditions, allowing selective transformations in multi-step synthetic pathways. Additionally, the 3-bromopropoxy moiety can act as a linker or spacer in the synthesis of bioactive compounds, enabling further functionalization or conjugation. This chemical is also utilized in the development of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular structure is critical. Its role in facilitating efficient and selective synthetic processes makes it a valuable tool in modern chemical research and industrial applications.
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