tert-Butyl 2-chloro-4-fluorobenzoate

98%

  • Product Code: 42893
  CAS:    911314-43-7
Molecular Weight: 230.6632 g./mol Molecular Formula: C₁₁H₁₂ClFO₂
EC Number: MDL Number: MFCD09800898
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex compounds. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of molecules with potential therapeutic properties. The presence of both chloro and fluoro substituents on the aromatic ring makes it a valuable building block for creating compounds with specific electronic and steric properties. Additionally, it is used in agrochemical research for the development of pesticides and herbicides, where the fluorine atom can enhance the biological activity of the final product. Its tert-butyl ester group also provides stability and can be easily removed or transformed during further chemical reactions, making it versatile for various synthetic pathways.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿900.00
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tert-Butyl 2-chloro-4-fluorobenzoate
This chemical is primarily utilized in organic synthesis as an intermediate for the production of more complex compounds. It is often employed in the pharmaceutical industry for the development of active pharmaceutical ingredients (APIs), particularly in the synthesis of molecules with potential therapeutic properties. The presence of both chloro and fluoro substituents on the aromatic ring makes it a valuable building block for creating compounds with specific electronic and steric properties. Additionally, it is used in agrochemical research for the development of pesticides and herbicides, where the fluorine atom can enhance the biological activity of the final product. Its tert-butyl ester group also provides stability and can be easily removed or transformed during further chemical reactions, making it versatile for various synthetic pathways.
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