3-Chloropropenyl-1-boronic acid pinacol ester
3-Chloropropenyl-1-boronic acid pinacol ester Basic information
- Product Name:
- 3-Chloropropenyl-1-boronic acid pinacol ester
- Synonyms:
-
- 3-Chloropropenyl-1-boronic acid pinacol ester
- 1,3,2-Dioxaborolane, 2-[(1E)-3-chloro-1-propen-1-yl]-4,4,5,5-tetramethyl-
- (E)-2-(3-Chloro-1-propenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 3-Chloropropenyl-1-boronic acid pinacol ester,2-(3-Chloro-propenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane
- 2-[(E)-3-chloroprop-1-enyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- (E)-2-(3-Chloroprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- 2-[(E)-3-chloroprop-1-en-1-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
- trans-2-Chloromethylvinylboronic acid pinacol ester 97%
- CAS:
- 153724-93-7
- MF:
- C9H16BClO2
- MW:
- 202.49
- Product Categories:
-
- Organoborons
- Mol File:
- 153724-93-7.mol
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3-Chloropropenyl-1-boronic acid pinacol ester Chemical Properties
- Density
- 1.028 g/mL at 25 °C
- refractive index
- n20/D1.4603
- Flash point:
- 100℃
- Boiling point:
- 57-62°C/0.3-0.4 mmHg
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3-Chloropropenyl-1-boronic acid pinacol ester Usage And Synthesis
Uses
trans-2-Chloromethylvinylboronic acid pinacol ester is a common reactant of Suzuki coupling reaction. It can be used to prepare:
- Readout reagent that helps in providing qualitative and quantitative readouts in enzyme biomarker detection assays.
- Boronated enynes, which on Au(I) catalyzed cycloisomerization yield various dienyl boronates.
- α-Methyl-substituted boronates for the allylation of ketones to yield homoallylic tertiary alcohols.
3-Chloropropenyl-1-boronic acid pinacol esterSupplier
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Sigma-Aldrich
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