tert-Butyl(3-iodophenoxy)dimethylsilane

97%

  • Product Code: 88534
  CAS:    133910-12-0
Molecular Weight: 334.27 g./mol Molecular Formula: C₁₂H₁₉IOSi
EC Number: MDL Number: MFCD00798178
Melting Point: Boiling Point: 286.9°C at 760 mmHg
Density: Storage Condition: -20°C, inert gas, dark
Product Description: This chemical is primarily used in organic synthesis as a protecting group for alcohols and phenols. Its silicon-based structure allows it to temporarily shield hydroxyl groups during complex reactions, preventing unwanted interactions. It is particularly useful in the synthesis of pharmaceuticals and fine chemicals, where selective protection and deprotection of functional groups are crucial. Additionally, it serves as an intermediate in the preparation of more complex organosilicon compounds, which are often employed in materials science and catalysis. The iodine atom in its structure also makes it a valuable building block for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings.
Product Specification:
Test Specification
APPEARANCE Colorless to Yellow Liquid
PURITY 96.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿1,000.00
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-
1.000 10-20 days ฿2,700.00
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-
5.000 10-20 days ฿9,440.00
+
-
25.000 10-20 days ฿33,000.00
+
-
tert-Butyl(3-iodophenoxy)dimethylsilane
This chemical is primarily used in organic synthesis as a protecting group for alcohols and phenols. Its silicon-based structure allows it to temporarily shield hydroxyl groups during complex reactions, preventing unwanted interactions. It is particularly useful in the synthesis of pharmaceuticals and fine chemicals, where selective protection and deprotection of functional groups are crucial. Additionally, it serves as an intermediate in the preparation of more complex organosilicon compounds, which are often employed in materials science and catalysis. The iodine atom in its structure also makes it a valuable building block for further functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings.
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