Tributyl(1-ethoxyvinyl)tin

97%

  • Product Code: 58463
  CAS:    97674-02-7
Molecular Weight: 361.15 g./mol Molecular Formula: C₁₆H₃₄OSn
EC Number: MDL Number: MFCD00010240
Melting Point: Boiling Point:
Density: 1.069g/cm3 Storage Condition: 2~8℃
Product Description: Tributyl(1-ethoxyvinyl)tin is primarily utilized in organic synthesis as a reagent for introducing the ethoxyvinyl group into various organic compounds. This chemical is particularly valuable in the preparation of vinyl ethers, which are important intermediates in the production of polymers, resins, and other specialty chemicals. It is also employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, where the ethoxyvinyl moiety can serve as a key functional group. Additionally, its role in cross-coupling reactions makes it useful in the development of advanced materials and fine chemicals. The compound's ability to facilitate selective transformations under mild conditions enhances its applicability in diverse synthetic pathways.
Product Specification:
Test Specification
Purity 96.5 100%
Appearance COLORLESS LIQUID
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿480.00
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5.000 10-20 days ฿980.00
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25.000 10-20 days ฿3,380.00
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100.000 10-20 days ฿12,530.00
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Tributyl(1-ethoxyvinyl)tin
Tributyl(1-ethoxyvinyl)tin is primarily utilized in organic synthesis as a reagent for introducing the ethoxyvinyl group into various organic compounds. This chemical is particularly valuable in the preparation of vinyl ethers, which are important intermediates in the production of polymers, resins, and other specialty chemicals. It is also employed in the synthesis of complex molecules, including pharmaceuticals and agrochemicals, where the ethoxyvinyl moiety can serve as a key functional group. Additionally, its role in cross-coupling reactions makes it useful in the development of advanced materials and fine chemicals. The compound's ability to facilitate selective transformations under mild conditions enhances its applicability in diverse synthetic pathways.
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