4-Carboxyphenylboronic acid
97%
- Product Code: 90726
Alias:
4-Carboxyphenylboronic acid
CAS:
14047-29-1
| Molecular Weight: | 165.94 g./mol | Molecular Formula: | C₇H₇BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151801 | |
| Melting Point: | 220 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
- Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds.
- Acts as a building block for the preparation of pharmaceutical compounds and bioactive molecules.
- Employed in the development of sensors and diagnostic tools due to its ability to bind with diols, such as sugars, for glucose monitoring.
- Utilized in the creation of advanced materials, including polymers and coatings with specific functional properties.
- Plays a role in research involving boron neutron capture therapy (BNCT) for cancer treatment.
- Applied in the study of molecular recognition and supramolecular chemistry for designing host-guest systems.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97-100 |
| APPEARANCE | White or light yellow powder |
| INFRARED SPECTRUM | Conforms to Structure |
| MELTING POINT | 220DEC |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $14.09 |
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| 5.000 | 10-20 days | $24.42 |
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| 25.000 | 10-20 days | $63.87 |
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| 100.000 | 10-20 days | $249.85 |
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| 500.000 | 10-20 days | $1,205.10 |
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4-Carboxyphenylboronic acid
- Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds.
- Acts as a building block for the preparation of pharmaceutical compounds and bioactive molecules.
- Employed in the development of sensors and diagnostic tools due to its ability to bind with diols, such as sugars, for glucose monitoring.
- Utilized in the creation of advanced materials, including polymers and coatings with specific functional properties.
- Plays a role in research involving boron neutron capture therapy (BNCT) for cancer treatment.
- Applied in the study of molecular recognition and supramolecular chemistry for designing host-guest systems.
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