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Product Name:2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol CAS:269409-97-4 Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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| 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL Basic information |
Product Name: | 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL | Synonyms: | 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol,min.97%;2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL, MIN. 97%;2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol,97%;2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, 2-(2-Hydroxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane;(3-hydroxy-2,3-dimethylbutan-2-yl)oxy-(2-hydroxyphenyl)borinic acid;Phenol, 2-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;2-(2-Hydroxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
2-Hydroxyphenylboronic Acid Pinacol Ester;2-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenol
2-Hydroxyphenylboronic Acid Pinacol Ester | CAS: | 269409-97-4 | MF: | C12H17BO3 | MW: | 220.07 | EINECS: | | Product Categories: | Boronic Acids and Derivatives;Chemical Synthesis;Organometallic Reagents;Aryl Boronate Esters;Boronate Esters;organic or inorganic borate;Boronic acids;B (Classes of Boron Compounds);Boronic Acids Esters | Mol File: | 269409-97-4.mol |  |
| 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL Chemical Properties |
Boiling point | 282 °C(lit.) | density | 1.05 g/mL at 25 °C(lit.) | refractive index | n20/D 1.506(lit.) | Fp | 230 °F | storage temp. | Keep in dark place,Sealed in dry,Room Temperature | Water Solubility | Insoluble in water | form | liquid | pka | 10.17±0.35(Predicted) | color | pale yellow | CAS DataBase Reference | 269409-97-4(CAS DataBase Reference) |
Hazard Codes | Xi,Xn | Risk Statements | 36/37/38-22 | Safety Statements | 26-36 | WGK Germany | 3 | Hazard Note | Irritant | TSCA | No | HS Code | 29319090 |
| 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL Usage And Synthesis |
Chemical Properties | pale yellow to brown liquid | Uses | 2-(4,4,5,5-TetraMethyl-1,3,2-dioxaborolan-2-yl)phenol can be widely used in Suzuki coupling chemistry. | Uses | Reactant involved in:
- Synthesis of indolo-fused heterocyclic inhibitors of polymerase enzyme of hepatitis C
- Studies of pi-interactions, electronic structure and transient UV absorption of subphthalocyanine-borate-bridged ferrocene-fullerene conjugates
- Synthesis of subphthalocyanine and fused-ring nicotine derivatives
- Suzuki-Miyaura coupling-triflation sequence, reduction and salt formation for synthesis of hydroxylated oligoarene phosphines
| Synthesis | GENERAL PROCEDURE: To a solution of o-aminophenol (0.5 mmol, 1.0 eq.) in methanol (1.0 mL) was added hydrochloric acid (0.5 mL, 1.5 mmol, 3.0 eq.) followed by water (0.5 mL). The mixture was stirred for 2 minutes and then sodium nitrite solution (0.25 mL) was added. Sodium nitrite solution was prepared by dissolving 35 mg of sodium nitrite in water (0.25 mL). The mixture was stirred at 0-5°C for 30 minutes, followed by the addition of a methanol (1.0 mL) solution of pinacol ester of bisboronic acid (2,381 mg, 1.5 mmol, 3.0 equiv). The reaction mixture was stirred for 60 minutes. Upon completion of the reaction, it was diluted with water (10 mL) and then extracted with dichloromethane (50 mL, 3 times). The organic layers were combined, washed with saturated sodium bicarbonate solution, dried over anhydrous sodium sulfate, concentrated and the crude product was purified by fast chromatography to give 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol. | References | [1] Synlett, 2014, vol. 25, # 11, p. 1577 - 1584 [2] Journal of Organic Chemistry, 2013, vol. 78, # 5, p. 1923 - 1933 |
| 2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENOL Preparation Products And Raw materials |
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