4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzeneethanol

≥95%

  • Product Code: 85097
  CAS:    651030-55-6
Molecular Weight: 248.13 g./mol Molecular Formula: C₁₄H₂₁BO₃
EC Number: MDL Number: MFCD18733921
Melting Point: Boiling Point: 363.2±25.0°C at 760 mmHg
Density: Storage Condition: 2-8°C, store under inert gas
Product Description: This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the synthesis of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in material science for the development of organic electronic materials, such as polymers and small molecules for OLEDs and other optoelectronic devices. The compound’s stability and reactivity make it a valuable tool in constructing aromatic systems and functionalized organic compounds.
Product Specification:
Test Specification
APPEARANCE White to Pale-yellow to Yellow-brown Sticky Oil to Semi-Solid
PURITY 95-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿960.00
+
-
0.250 10-20 days ฿1,930.00
+
-
1.000 10-20 days ฿4,860.00
+
-
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzeneethanol
This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the production of complex organic molecules. Its application is significant in pharmaceutical research, where it aids in the synthesis of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in material science for the development of organic electronic materials, such as polymers and small molecules for OLEDs and other optoelectronic devices. The compound’s stability and reactivity make it a valuable tool in constructing aromatic systems and functionalized organic compounds.
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