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| 4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET& Basic information |
| Product Name: | 4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET& | | Synonyms: | 4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET&;Phenylthiomethylboronic acid pinacol ester;1,3,2-Dioxaborolane, 4,4,5,5-tetramethyl-2-[(phenylthio)methyl]-;4,4,5,5,-Tetramethyl-2-phenylsulfanylmethyl-1,3,2-dioxaborolane 97%;4,4,5,5-Tetramethyl-2-(phenylthiomethyl)-1,3,2-dioxaborolane | | CAS: | 66080-23-7 | | MF: | C13H19BO2S | | MW: | 250.16 | | EINECS: | | Product Categories: | Aryl;Organoborons;Thio;Boronate Esters;Boronic Acids and Derivatives | | Mol File: | 66080-23-7.mol |
| 4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET& Chemical Properties |
| 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 |
| 4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET& Usage And Synthesis |
| 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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| 4 4 5 5-TETRAMETHYL-2-PHENYLSULFANYLMET& Preparation Products And Raw materials |
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