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1029684-36-3

1029684-36-3 Structure

1029684-36-3 Structure
IdentificationBack Directory
[Name]

2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic acid pinacol ester
[CAS]

1029684-36-3
[Synonyms]

2-Chloro-1-(tetrahydro-py...
2-chloro-1-(oxan-2-yl)-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-imidazole
2-Chloro-1-(tetrahydro-pyran-2-yl)-1H-iMidazole-5-boronic acid pinacol ester
2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic acid pinacol ester
2-Chloro-1-(oxan-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazole
2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole
1H-Imidazole, 2-chloro-1-(tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C14H22BClN2O3
[MDL Number]

MFCD11100958
[MOL File]

1029684-36-3.mol
[Molecular Weight]

312.6
Chemical PropertiesBack Directory
[Melting point ]

135 °C
[Boiling point ]

466.0±55.0 °C(Predicted)
[density ]

1.25±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[pka]

3.72±0.70(Predicted)
[Appearance]

White to off-white Solid
Hazard InformationBack Directory
[Uses]

2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic Acid Pinacol Ester is derived from 2-Chlorotetrahydro-2H-pyran (C433055), which is commonly used starting material in organic synthesis.
Spectrum DetailBack Directory
[Spectrum Detail]

2-Chloro-1-(tetrahydro-2H-pyran-2-yl)-1H-imidazole-5-boronic acid pinacol ester(1029684-36-3)1HNMR
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