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
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
Purity 94.5-100
Appearance Colorless to yellow to orange liquid
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
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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