tert-Butyl(3-iodophenoxy)dimethylsilane
97%
- Product Code: 88534
CAS:
133910-12-0
Molecular Weight: | 334.27 g./mol | Molecular Formula: | C₁₂H₁₉IOSi |
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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 |
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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 |
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25.000 | 10-20 days | ฿33,000.00 |
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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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