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183288-43-9

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183288-43-9 Structure

183288-43-9 Structure
IdentificationBack Directory
[Name]

Ethyl 5-(4-tert-butoxycarbonyl-1-piperazinyl)benzofuran-2-carboxylate
[CAS]

183288-43-9
[Synonyms]

EOS-60443
1-Boc-4-(2-(ethoxycarbonyl)benzofuran-5-yl)piperazine
Ethyl 5-(4-tert-butoxycarbonyl-1-piperazinyl)benzofuran-2-carboxylate
tert-Butyl 4-(2-(ethoxycarbonyl)benzofuran-5-yl)piperazine-1-carboxylate
ethyl 5-(4-tert-butoxycarbonyl-1-piperazinyl)benzofuran-2-carboxylate(C3)
tert-butyl 4-(2-ethoxycarbonyl-1-benzofuran-5-yl)piperazine-1-carboxylate
4-[2-(Ethoxycarbonyl)-5-benzofuranyl]-1-piperazinecarboxylic acid tert-butyl ester
1-Piperazinecarboxylic acid, 4-[2-(ethoxycarbonyl)-5-benzofuranyl]-, 1,1-diMethylethyl ester
[EINECS(EC#)]

695-998-3
[Molecular Formula]

C20H26N2O5
[MDL Number]

MFCD21607421
[MOL File]

183288-43-9.mol
[Molecular Weight]

374.431
Chemical PropertiesBack Directory
[Boiling point ]

494.0±45.0 °C(Predicted)
[density ]

1.202
[storage temp. ]

Sealed in dry,2-8°C
[pka]

0.13±0.70(Predicted)
Questions And AnswerBack Directory
[Uses]

Ethyl 5-(4-tert-butoxycarbonyl-piperazin-1-yl)benzofuran-2-carboxylate can be used to prepare 5-(1-piperazinyl)-benzofuran-2-carboxamide. 5-(1-piperazinyl)-benzofuran-2-carboxamide or its acid addition salt is a key intermediate in the synthesis of vilazone.
Safety DataBack Directory
[Symbol(GHS) ]

Environment (GHS09)
GHS09
[Hazard statements ]

H411
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