(1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroquinolin-6-yl)boronic acid
98%
- Product Code: 152135
CAS:
1260150-04-6
| Molecular Weight: | 277.12 g./mol | Molecular Formula: | C₁₄H₂₀BNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06801709 | |
| Melting Point: | Boiling Point: | 453.3±55.0 °C(Predicted) | |
| Density: | 1.21±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecule assembly. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and reactivity of the boronic acid group. The tert-butoxycarbonyl (Boc) protecting group enhances solubility and stability during reaction sequences, making it suitable for multi-step syntheses. Frequently utilized in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $80.82 |
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| 0.250 | 10-20 days | $154.91 |
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| 1.000 | 10-20 days | $526.38 |
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| 5.000 | 10-20 days | $2,281.67 |
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(1-(tert-Butoxycarbonyl)-1,2,3,4-tetrahydroquinolin-6-yl)boronic acid
Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecule assembly. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and reactivity of the boronic acid group. The tert-butoxycarbonyl (Boc) protecting group enhances solubility and stability during reaction sequences, making it suitable for multi-step syntheses. Frequently utilized in the preparation of drug candidates targeting cancer, inflammation, and central nervous system disorders.
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