Ethyl 2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate

98%

  • Product Code: 83496
  CAS:    850411-07-3
Molecular Weight: 306.16 g./mol Molecular Formula: C₁₆H₂₃BO₅
EC Number: MDL Number: MFCD06657707
Melting Point: Boiling Point: 405.1±25.0°C at 760 mmHg
Density: Storage Condition: Room temperature, airtight, dry
Product Description: This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the ethoxycarbonylmethyl group enhances its reactivity and versatility in forming carbon-carbon bonds. Additionally, it is often used in the development of bioactive compounds and in the modification of organic frameworks for material science applications. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic and synthetic processes.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $203.51
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0.250 10-20 days $306.15
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1.000 10-20 days $762.37
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Ethyl 2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)acetate
This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules. Its boronate ester functionality makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The presence of the ethoxycarbonylmethyl group enhances its reactivity and versatility in forming carbon-carbon bonds. Additionally, it is often used in the development of bioactive compounds and in the modification of organic frameworks for material science applications. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic and synthetic processes.
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