N,N-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-propanamine
97%
- Product Code: 121300
CAS:
847818-72-8
| Molecular Weight: | 279.19 g./mol | Molecular Formula: | C₁₄H₂₆BN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11983295 | |
| Melting Point: | Boiling Point: | 383.9°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its pyrazole moiety is often leveraged in drug discovery for creating compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer properties. The presence of the dimethylamine group further enhances its utility in modifying the physicochemical properties of target molecules, improving solubility or bioavailability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,961.00 |
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| 0.250 | 10-20 days | ฿5,076.00 |
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| 1.000 | 10-20 days | ฿11,844.00 |
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N,N-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole-1-propanamine
This chemical is primarily utilized in organic synthesis as a versatile building block, particularly in the development of pharmaceuticals and agrochemicals. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its pyrazole moiety is often leveraged in drug discovery for creating compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer properties. The presence of the dimethylamine group further enhances its utility in modifying the physicochemical properties of target molecules, improving solubility or bioavailability.
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