3-Chloro-4-methylphenylboronic acid

97%

  • Product Code: 90211
  Alias:    3-Chloro-4-methylphenylboronic acid
  CAS:    175883-63-3
Molecular Weight: 170.4 g./mol Molecular Formula: C₇H₈BClO₂
EC Number: MDL Number: MFCD04039010
Melting Point: 210-216°C Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: 3-Chloro-4-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.
Product Specification:
Test Specification
Melting point 223-230
PURITYHPLC 97-100
APPEARANCE White crystalline powder
INFRARED SPECTRUM CONFORMS
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿570.00
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-
5.000 10-20 days ฿1,760.00
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-
25.000 10-20 days ฿6,740.00
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-
3-Chloro-4-methylphenylboronic acid
3-Chloro-4-methylphenylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and polymers. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse aromatic structures. Additionally, it is employed in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.
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