4-Acetoxyphenylboronic acid pinacol ester

97%

  • Product Code: 90552
  Alias:    4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate
  CAS:    480424-70-2
Molecular Weight: 262.11 g./mol Molecular Formula: C₆H₄OCOCH₃BO₂C₂CH₃₄
EC Number: MDL Number: MFCD03453060
Melting Point: 67-71 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: Used in organic synthesis as a key intermediate for the preparation of various bioactive molecules and pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic compounds. This chemical is also employed in the development of sensors and probes for detecting specific analytes due to its boronic acid functionality, which can selectively bind to diols and sugars. Additionally, it finds application in material science for the modification of surfaces and the creation of functionalized polymers.
Product Specification:
Test Specification
Melting point 67-71
PURITY HPLC 97-100
APPEARANCE White to off-white powder
INFRARED SPECTROMETRY Conforms to Structure
PROTON NMR SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days ฿1,350.00
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-
1.000 10-20 days ฿2,230.00
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-
5.000 10-20 days ฿8,900.00
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-
25.000 10-20 days ฿39,880.00
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-
4-Acetoxyphenylboronic acid pinacol ester
Used in organic synthesis as a key intermediate for the preparation of various bioactive molecules and pharmaceuticals. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic compounds. This chemical is also employed in the development of sensors and probes for detecting specific analytes due to its boronic acid functionality, which can selectively bind to diols and sugars. Additionally, it finds application in material science for the modification of surfaces and the creation of functionalized polymers.
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