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457613-78-4

457613-78-4 Structure

457613-78-4 Structure
IdentificationBack Directory
[Name]

(4-[4-(TERT-BUTOXYCARBONYL)PIPERAZIN-1-YL]PHENYL)BORONIC ACID
[CAS]

457613-78-4
[Synonyms]

4-(4-BOC-Piperazino)phenylboronic acid
4-(4-Boc-1-piperazinyl)phenylboronic Acid
(4-[4-(TERT-BUTOXYCARBONYL)PIPERAZIN-1-YL]PHENYL)BORONIC ACID
[4-[4-[(2-methylpropan-2-yl)oxycarbonyl]piperazin-1-yl]phenyl]boronic acid
[4-[4-[(2-methylpropan-2-yl)oxy-oxomethyl]-1-piperazinyl]phenyl]boronic acid
1-Piperazinecarboxylic acid, 4-(4-boronophenyl)-, 1-(1,1-diMethylethyl) ester
[Molecular Formula]

C15H23BN2O4
[MDL Number]

MFCD10696663
[MOL File]

457613-78-4.mol
[Molecular Weight]

306.17
Chemical PropertiesBack Directory
[Melting point ]

187-189 °C
[Boiling point ]

487.4±55.0 °C(Predicted)
[density ]

1.21±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

9.08±0.17(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P362+P364
Hazard InformationBack Directory
[Uses]

4-(4-BOC-Piperazino)phenylboronic acid acts as a reagent in the synthesis of hydroxyaniline amides as selective extracellular regulated Kinase (Erk) inhibitors, preparation of 3,5-disubstituted indole derivatives as potent inhibitors of pim-1, pim-2, pim-3 protein kinase.
Spectrum DetailBack Directory
[Spectrum Detail]

(4-[4-(TERT-BUTOXYCARBONYL)PIPERAZIN-1-YL]PHENYL)BORONIC ACID(457613-78-4)1HNMR
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