tributyl-(3,5-difluoropyridin-4-yl)stannane

95%

  • Product Code: 58430
  CAS:    765916-82-3
Molecular Weight: 404.117 g./mol Molecular Formula: C₁₇H₂₉F₂NSn
EC Number: MDL Number: MFCD09025762
Melting Point: Boiling Point: 363.899ºC at 760 mmHg
Density: Storage Condition: 2-8℃
Product Description: Tributyl-(3,5-difluoropyridin-4-yl)stannane is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. Its application is particularly significant in the field of medicinal chemistry, where it is used to introduce the 3,5-difluoropyridinyl moiety into target compounds. This moiety is often incorporated into drug candidates to enhance their binding affinity and metabolic stability. Additionally, the compound is employed in the development of agrochemicals, where the difluoropyridinyl group can improve the efficacy and selectivity of pesticides and herbicides. In material science, it serves as a building block for the synthesis of advanced materials, including polymers and coatings, which benefit from the unique electronic properties of the difluoropyridinyl group.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿1,791.00
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1.000 10-20 days ฿11,241.00
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tributyl-(3,5-difluoropyridin-4-yl)stannane
Tributyl-(3,5-difluoropyridin-4-yl)stannane is primarily utilized in organic synthesis as a key intermediate for the preparation of more complex molecules. Its application is particularly significant in the field of medicinal chemistry, where it is used to introduce the 3,5-difluoropyridinyl moiety into target compounds. This moiety is often incorporated into drug candidates to enhance their binding affinity and metabolic stability. Additionally, the compound is employed in the development of agrochemicals, where the difluoropyridinyl group can improve the efficacy and selectivity of pesticides and herbicides. In material science, it serves as a building block for the synthesis of advanced materials, including polymers and coatings, which benefit from the unique electronic properties of the difluoropyridinyl group.
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