(5-Fluorobenzofuran-2-yl)boronic acid
- Product Name
- (5-Fluorobenzofuran-2-yl)boronic acid
- CAS No.
- 473416-33-0
- Chemical Name
- (5-Fluorobenzofuran-2-yl)boronic acid
- Synonyms
- 5-fluorobenzofuran-2-boronic acid;(5-Flufuran-2-based) boronic acid;5-Fluorobenzofurane-2-boronic Acid;(5-Fluorobenzofuran-2-yl)boronic acid;Boronic acid, (5-fluoro-2-benzofuranyl)- (9CI)
- CBNumber
- CB32710128
- Molecular Formula
- C8H6BFO3
- Formula Weight
- 179.94
- MOL File
- 473416-33-0.mol
(5-Fluorobenzofuran-2-yl)boronic acid Property
- Boiling point:
- 343.8±45.0 °C(Predicted)
- Density
- 1.40±0.1 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Store in freezer, under -20°C
- pka
- 5.88±0.30(Predicted)
- Appearance
- White to off-white Solid
Safety
- HS Code
- 2932990090
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- F593865
- Product name
- (5-Fluoro-2-benzofuranyl)boronicAcid
- Packaging
- 10mg
- Price
- $150
- Updated
- 2021/12/16
- Product number
- PC535073
- Product name
- (5-Fluorobenzofuran-2-yl)boronicacid
- Purity
- 98%
- Packaging
- 100mg
- Price
- $60
- Updated
- 2021/12/16
- Product number
- PC535073
- Product name
- (5-Fluorobenzofuran-2-yl)boronicacid
- Purity
- 98%
- Packaging
- 250mg
- Price
- $96
- Updated
- 2021/12/16
- Product number
- 1650DA
- Product name
- (5-Fluorobenzofuran-2-yl)boronicacid
- Packaging
- 250mg
- Price
- $222
- Updated
- 2021/12/16
- Product number
- 1650DA
- Product name
- (5-Fluorobenzofuran-2-yl)boronicacid
- Packaging
- 1g
- Price
- $431
- Updated
- 2021/12/16
(5-Fluorobenzofuran-2-yl)boronic acid Chemical Properties,Usage,Production
Uses
(5-Fluoro-2-benzofuranyl)boronic Acid serves as a reagent for the preparation of heterocyclic compounds for the inhibition of PASK useful for the treatment of diseases like diabetes mellitus.
Synthesis
24410-59-1
5419-55-6
473416-33-0
Step 3. Synthesis of (5-fluorofuran-2-yl)boronic acid Tetramethylethylenediamine (10.2 g, 87.93 mmol) was added to an anhydrous tetrahydrofuran (250 mL) solution of 5-fluorobenzofuran (10 g, 73.53 mmol). The reaction system was cooled to below -60 °C under nitrogen protection and n-butyllithium (93.75 mmol, 2.5 M hexane solution) was slowly added dropwise. After the dropwise addition, the reaction mixture was slowly warmed up to -10 °C over 45 min and stirring was continued at this temperature for 30 min. Subsequently, the reaction system was cooled again to below -60°C and triisopropyl borate (41.4 g, 220.21 mmol) was slowly added dropwise. After completion of the dropwise addition, the reaction mixture was gradually warmed to room temperature, the reaction was quenched with 2N hydrochloric acid (70 mL) and stirred for 1 hour. The pH of the aqueous layer was adjusted to 5 with sodium hydroxide solution and extracted with ethyl acetate (3 x 80 mL). The organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to afford the crude product (5-fluorofuran-2-yl)boronic acid (3.5 g, 26% yield), which could be used in the next reaction without further purification. 1H-NMR (300MHz, CDCl3): δ8.63 (s, 2H), 7.58-7.62 (m, 1H), 7.44-7.49 (m, 2H), 7.15-7.22 (m, 1H).
References
[1] Patent: US2012/225863, 2012, A1. Location in patent: Page/Page column 17-18
(5-Fluorobenzofuran-2-yl)boronic acid Preparation Products And Raw materials
Raw materials
Preparation Products
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