2,6-Dimethylbenzeneboronic acid

98%

  • Product Code: 89597
  Alias:    2,6-Dimethylphenylboronic acid
  CAS:    100379-00-8
Molecular Weight: 149.98 g./mol Molecular Formula: C₈H₁₁BO₂
EC Number: MDL Number: MFCD01009693
Melting Point: 105 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used primarily in organic synthesis, it serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of complex organic molecules, including potential drug candidates. Additionally, it is employed in the production of advanced materials, such as organic semiconductors and polymers, due to its ability to modify and stabilize molecular structures. Its applications extend to research laboratories where it aids in the study of new chemical reactions and pathways.
Product Specification:
Test Specification
Melting point 120-126
PURITYHPLC 98-100
APPEARANCE POWDER FLAKES,CRYSTALS,SOLID AND/OR CHUNKS
INFRARED SPECTRUM Conforms to Structure
PROTON NMR SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $15.78
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5.000 10-20 days $49.42
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25.000 10-20 days $217.61
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-
100.000 10-20 days $829.75
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2,6-Dimethylbenzeneboronic acid
Used primarily in organic synthesis, it serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This makes it valuable in the development of complex organic molecules, including potential drug candidates. Additionally, it is employed in the production of advanced materials, such as organic semiconductors and polymers, due to its ability to modify and stabilize molecular structures. Its applications extend to research laboratories where it aids in the study of new chemical reactions and pathways.
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