| Identification | Back Directory | [Name]
4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET& | [CAS]
66080-23-7 | [Synonyms]
4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET&
Phenylthiomethylboronic acid pinacol ester
4,4,5,5-Tetramethyl-2-(phenylthiomethyl)-1,3,2-dioxaborolane
1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(phenylthio)methyl]-
4,4,5,5,-Tetramethyl-2-phenylsulfanylmethyl-1,3,2-dioxaborolane 97% | [Molecular Formula]
C13H19BO2S | [MDL Number]
MFCD08669621 | [MOL File]
66080-23-7.mol | [Molecular Weight]
250.16 |
| Chemical Properties | Back Directory | [Boiling point ]
105-108 °C/0.1 mmHg (lit.) | [density ]
1.059 g/mL at 25 °C (lit.) | [refractive index ]
n20/D 1.5280(lit.) | [Fp ]
221 °F | [InChI]
1S/C13H19BO2S/c1-12(2)13(3,4)16-14(15-12)10-17-11-8-6-5-7-9-11/h5-9H,10H2,1-4H3 | [InChIKey]
DGPGLPBMZOKGON-UHFFFAOYSA-N | [SMILES]
CC1(C)OB(CSc2ccccc2)OC1(C)C |
| Hazard Information | Back Directory | [Uses]
4,4,5,5,-Tetramethyl-2-phenylsulfanylmethyl-1,3,2-dioxaborolane is used to prepare aryl/heteroaryl derivatives via the formation of C-C and C-hetero bonds.
It can also be used as:
- A starting material in the synthesis of α-aminoboronic acids as serine proteases inhibitors.
- A substrate in the coupling reactions with carbonyl compounds under Ir-catalyzed photoredox conditions.
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