| Identification | More | [Name]
(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZENE | [CAS]
24388-23-6 | [Synonyms]
M7121
Phenylpinacolborane
(Pinacolboryl)benzene
Pinacol phenylboronate
PHENYL-BORONIC ACID PINACOL ESTER
Benzeneboronic acid, pinacol ester
Phenylboronic acid pinacol ester 97%
(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-
4,4,5,5-Tetramethyl-2-phenyl-1,3,2-dioxaborolane
2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
1,3,2-Dioxaborolane,4,4,5,5-tetraMethyl-2-phenyl-
2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane>
cyclic tetramethylethylene ester benzeneboronic acid
(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)BENZENE
(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzene
Phenylboronic Acid Pinacol Ester
(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 2-Phenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane | [Molecular Formula]
C12H17BO2 | [MDL Number]
MFCD00966985 | [Molecular Weight]
204.07 | [MOL File]
24388-23-6.mol |
| Chemical Properties | Back Directory | [Melting point ]
27-31 °C(lit.)
| [Boiling point ]
130°C/20mmHg(lit.) | [density ]
0.99±0.1 g/cm3(Predicted) | [Fp ]
225 °F
| [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [form ]
powder to lump | [color ]
White to Almost white | [InChIKey]
KKLCYBZPQDOFQK-UHFFFAOYSA-N | [CAS DataBase Reference]
24388-23-6(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R22:Harmful if swallowed.
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HS Code ]
29319090 |
| Hazard Information | Back Directory | [Chemical Properties]
White to light yellow crystal | [Uses]
suzuki reaction | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 60, p. 7508, 1995 DOI: 10.1021/jo00128a024 | [General Description]
Phenylboronic acid, pinacol ester, also known as boronate ester, is generally used in metal-catalyzed C-C bond formation reactions like Suzuki–Miyaura?reaction. |
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