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ChemicalBook--->CAS DataBase List--->24388-23-6

24388-23-6

24388-23-6 Structure

24388-23-6 Structure
IdentificationMore
[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 PropertiesBack 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
[InChIKey]

KKLCYBZPQDOFQK-UHFFFAOYSA-N
[CAS DataBase Reference]

24388-23-6(CAS DataBase Reference)
Safety DataBack 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 InformationBack 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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