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| 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester Basic information |
Product Name: | 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester | Synonyms: | 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester;1-Isopropylpyrazole-5-boronic Acid Pinacol Ester;(1-Isopropyl-1H-Pyrazol-5-YL)Boronic Acid Pinacol Ester;3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (1-isopropyl-1H-pyrazol-5-yl)boronate;1-Isopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl);1H-Pyrazole, 1-(1-Methylethyl)-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;1-(propan-2-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole;1-(1-Methylethyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | CAS: | 1282518-60-8 | MF: | C12H21BN2O2 | MW: | 236.12 | EINECS: | | Product Categories: | | Mol File: | 1282518-60-8.mol | |
| 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester Chemical Properties |
Boiling point | 327.3±15.0 °C(Predicted) | density | 1.03±0.1 g/cm3(Predicted) | storage temp. | Inert atmosphere,Store in freezer, under -20°C | pka | 1.98±0.10(Predicted) | form | solid | color | White to off-white |
| 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester Usage And Synthesis |
Synthesis | 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester could be synthesized through the reaction of 1-isopropyl-1H-pyrazole with 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Tetrahydrofuran could used as an organic solvent. The crude product added n-hexane, heated to 40°C to dissolve the system, cooled to -20°C, stirred and crystallized, and filtered. Vacuum drying to obtain the target compound 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester, with a yield of 77% and a purity of 99.3%.
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| 1-Isopropyl-1H-pyrazole-5-boronic acid, pinacol ester Preparation Products And Raw materials |
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