ChemicalBook--->CAS DataBase List--->70557-99-2

70557-99-2

70557-99-2 Structure

70557-99-2 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P271-P280
[HS Code ]

2931900090
Hazard InformationBack 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]

(Bromomethyl)boronic Acid Pinacol Ester

166330-03-6

Iodomethylboronic acid, pinacol ester

70557-99-2

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
Spectrum DetailBack Directory
[Spectrum Detail]

Iodomethylboronic acid, pinacol ester(70557-99-2)1HNMR
Iodomethylboronic acid, pinacol ester(70557-99-2)FT-IR
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