- 3-ETHYLPHENYLBORONIC ACID
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- $34.00 / 1kg
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2025-09-25
- CAS:90555-65-0
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: g-kg-tons, free sample is available
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| | 3-ETHYLPHENYLBORONIC ACID Basic information |
| | 3-ETHYLPHENYLBORONIC ACID Chemical Properties |
| Melting point | 102.5-107.5 C | | Boiling point | 299.6±33.0 °C(Predicted) | | density | 1.07±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | | form | solid | | pka | 8.62±0.10(Predicted) | | color | White | | InChI | 1S/C8H11BO2/c1-2-7-4-3-5-8(6-7)9(10)11/h3-6,10-11H,2H2,1H3 | | InChIKey | JIMVRUCDZGFJRE-UHFFFAOYSA-N | | SMILES | CCc1cccc(c1)B(O)O |
| Hazard Codes | Xi | | Risk Statements | 36/37/38-36/38 | | Safety Statements | 26-36/37 | | WGK Germany | 3 | | HS Code | 2931900090 | | Storage Class | 11 - Combustible Solids | | Hazard Classifications | Eye Irrit. 2
Skin Irrit. 2 |
| | 3-ETHYLPHENYLBORONIC ACID Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of 3-ethylphenylboronic acid from 3-bromoethylbenzene was as follows: 1-bromo-3-ethylbenzene (2.80 g, 15 mmol) was dissolved in tetrahydrofuran (40 mL) under nitrogen protection, cooled to -78 °C and stirred. n-Butyllithium (10 mL, 16 mmol) was slowly added and stirring was continued for 10 minutes. Subsequently, triisopropyl borate (6.92 mL, 30 mmol) was added and the reaction mixture was allowed to gradually warm to room temperature. Upon completion of the reaction, 1 M hydrochloric acid (50 mL) was added for acidification and then extracted with ether (100 mL). The organic phase was dried with anhydrous sodium sulfate, filtered and concentrated. The crude product was purified by recrystallization in water and washed with hexane to give 0.591 g of 3-ethylphenylboronic acid in 26% yield. Mass spectrometry analysis showed (M + ACN)+ peak of 195. | | References | [1] Journal of Organic Chemistry, 2000, vol. 65, # 10, p. 3200 - 3206
[2] Patent: WO2006/9876, 2006, A2. Location in patent: Page/Page column 183 |
| | 3-ETHYLPHENYLBORONIC ACID Preparation Products And Raw materials |
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