tert-Butyl(4-iodobutoxy)diMethylsilane
95%
- Product Code: 88535
Alias:
(4-iodobutoxy) tert-butyldimethylsilane;
CAS:
92511-12-1
Molecular Weight: | 314.28 g./mol | Molecular Formula: | C₁₀H₂₃IOSi |
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EC Number: | MDL Number: | MFCD01863695 | |
Melting Point: | Boiling Point: | 75ºC | |
Density: | 1.214g/cm3 | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used in organic synthesis as a protective group for alcohols. The tert-butyldimethylsilyl (TBDMS) group is introduced to shield hydroxyl groups during complex multi-step reactions, ensuring selective reactivity of other functional groups. Its application is particularly valuable in the synthesis of natural products, pharmaceuticals, and complex organic molecules, where precise control over reactivity is crucial. Additionally, the iodine moiety in the structure allows for further functionalization, making it a versatile intermediate in coupling reactions and other transformations. Its stability under various reaction conditions makes it a reliable choice for protecting sensitive alcohols in synthetic chemistry.
Product Specification:
Test | Specification |
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Purity | 94.5-100 |
Appearance | Colorless to yellow to orange liquid |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿780.00 |
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1.000 | 10-20 days | ฿2,580.00 |
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5.000 | 10-20 days | ฿7,980.00 |
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25.000 | 10-20 days | ฿22,880.00 |
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tert-Butyl(4-iodobutoxy)diMethylsilane
This chemical is primarily used in organic synthesis as a protective group for alcohols. The tert-butyldimethylsilyl (TBDMS) group is introduced to shield hydroxyl groups during complex multi-step reactions, ensuring selective reactivity of other functional groups. Its application is particularly valuable in the synthesis of natural products, pharmaceuticals, and complex organic molecules, where precise control over reactivity is crucial. Additionally, the iodine moiety in the structure allows for further functionalization, making it a versatile intermediate in coupling reactions and other transformations. Its stability under various reaction conditions makes it a reliable choice for protecting sensitive alcohols in synthetic chemistry.
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