2-Methoxycarbonylindole-5-boronicacid
- Product Name
- 2-Methoxycarbonylindole-5-boronicacid
- CAS No.
- 284660-86-2
- Chemical Name
- 2-Methoxycarbonylindole-5-boronicacid
- Synonyms
- 2-Methoxycarbonylindole-5-boronicacid;[2-(Methoxycarbonyl)-1H-indol-5-yl]boronic acid;1H-Indole-2-carboxylic acid, 5-borono-, 2-methyl ester;methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylate
- CBNumber
- CB21450813
- Molecular Formula
- C10H10BNO4
- Formula Weight
- 219
- MOL File
- 284660-86-2.mol
2-Methoxycarbonylindole-5-boronicacid Property
- Boiling point:
- 484.2±48.0 °C(Predicted)
- Density
- 1.39±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 8.55±0.30(Predicted)
- Appearance
- Light yellow to yellow Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
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
- BOR0005721
- Product name
- 2-METHOXYCARBONYLINDOLE-5-BORONIC ACID
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $502.01
- Updated
- 2021/12/16
- Product number
- 2795AB
- Product name
- 2-Methoxycarbonylindole-5-boronicacid
- Packaging
- 250mg
- Price
- $579
- Updated
- 2021/12/16
- Product number
- 096362
- Product name
- 2-Methoxycarbonylindole-5-boronic acid
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $591
- Updated
- 2021/12/16
- Product number
- BOR0005721
- Product name
- 2-METHOXYCARBONYLINDOLE-5-BORONIC ACID
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $1274.7
- Updated
- 2021/12/16
- Product number
- 096362
- Product name
- 2-Methoxycarbonylindole-5-boronic acid
- Purity
- 95+%
- Packaging
- 1g
- Price
- $1311
- Updated
- 2021/12/16
2-Methoxycarbonylindole-5-boronicacid Chemical Properties,Usage,Production
Synthesis
284660-89-5
111-42-2
284660-86-2
General procedure for the synthesis of (2-(methoxycarbonyl)-1H-indol-5-yl)boronic acid from methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylate and diethanolamine: 1. 391.2 mg (1.3 mmol) of methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylate was dissolved in ethyl acetate (EtOAc). 2. 0.25 mL (2.6 mmol) of diethanolamine was added to the solution and the reaction mixture was stirred overnight at room temperature. 3. Upon completion of the reaction, the white precipitate formed was collected by filtration. 4. The white precipitate was sonicated in 1N hydrochloric acid (HCl). 5. The treated white precipitate was again collected by filtration and dissolved in methanol (MeOH). 6. The methanol solution was concentrated in vacuum to afford the target product (2-(methoxycarbonyl)-1H-indol-5-yl)boronic acid with a recovery of 36.6 mg (13% yield). Product Characterization: HPLC retention time (Rf) = 13.912 min. 1H NMR (DMSO-d6, δ): 3.85 (s, 3H), 7.15 (s, 1H), 7.36 (d, J = 8.4 Hz, 1H), 7.67 (d, J = 8.4 Hz, 1H), 7.87 (s, 1H), 8.14 (s, 1H), 11.91 (s, 1H).
References
[1] Patent: US2008/4241, 2008, A1. Location in patent: Page/Page column 140-141
2-Methoxycarbonylindole-5-boronicacid Preparation Products And Raw materials
Raw materials
Preparation Products
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