| Identification | Back Directory | [Name]
Iodomethylboronic acid, pinacol ester | [CAS]
70557-99-2 | [Synonyms]
Iodomethylboronic acid, pinacol ester 2-(Iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 1,3,2-Dioxaborolane, 2-(iodoMethyl)-4,4,5,5-tetraMethyl- | [Molecular Formula]
C7H14BIO2 | [MDL Number]
MFCD12405515 | [MOL File]
70557-99-2.mol | [Molecular Weight]
267.9 |
| Chemical Properties | Back Directory | [Boiling point ]
64-65 °C(Press: 0.2 Torr) | [density ]
1.47±0.1 g/cm3(Predicted) | [storage temp. ]
Keep in dark place,Inert atmosphere,Store in freezer, under -20°C | [form ]
Chloroform, Dichloromethane | [Appearance]
Light yellow to brown Liquid | [InChIKey]
UBNNPAYFVZFWPE-UHFFFAOYSA-N |
| Hazard Information | Back Directory | [Chemical Properties]
Chloroform, Dichloromethane | [Uses]
Iodomethylboronic acid pinacol esterUsed is in the preparation of Taspase1 inhibitors and α-methylene-γ-butyrolactones. α-Methylene-γ-butyrolactones have the ability to suppress growth in pancreatic carcinoma cells.
| [Uses]
Used in the preparation of Taspase1 inhibitors and α-methylene-γ-butyrolactones. α-Methylene-γ-butyrolactones have the ability to suppress growth in pancreatic carcinoma cells. | [Synthesis]
The general procedure for the synthesis of iodomethylboronic acid pinacol ester from bromomethylboronic acid pinacol ester is as follows:[Example 22] Synthesis of 2-(iodomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.0 g, 8.3 mmol) was mixed with acetone (17 ml), sodium iodide (1.9 g, 13 mmol) was added, and the reaction mixture was stirred for 2 hours at room temperature. After completion of the reaction, the insoluble impurities were removed by filtration and the filtrate was concentrated under reduced pressure to remove the solvent. Hexane was added to the residue and filtered to remove insoluble matter. Finally, the solvent was evaporated under reduced pressure to afford the target product pinacol ester of iodomethylboronic acid (2.2 g, 97% yield). The product was characterized by 1H-NMR (CDCl3): δ 1.29 (12H, s), 2.59 (2H, s). | [References]
[1] Patent: EP2062901, 2009, A1. Location in patent: Page/Page column 21-22 |
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Energy Chemical
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021-021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
SynAsst Chemical.
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021-60343070 |
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www.chemicalbook.com/ShowSupplierProductsList15848/0_EN.htm |
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