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220223-46-1

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220223-46-1 Structure

220223-46-1 Structure
IdentificationBack Directory
[Name]

Methyl N-Boc-3-Oxopiperidine-4-carboxylate
[CAS]

220223-46-1
[Synonyms]

Methyl N-Boc-3-Oxopiperidine-4-carboxylate
Methyl N-tert-Butoxycarbonyl-3-Oxopiperidine-4-carboxylate
3-Oxo-1,4-piperidinedicarboxylic acid 1-(1,1-dimethylethyl) 4-methyl ester
1,4-Piperidinedicarboxylic acid, 3-oxo-, 1-(1,1-diMethylethyl) 4-Methyl ester
[Molecular Formula]

C12H19NO5
[MDL Number]

MFCD12198882
[MOL File]

220223-46-1.mol
[Molecular Weight]

257.28
Chemical PropertiesBack Directory
[Boiling point ]

350.0±42.0 °C(Predicted)
[density ]

1.175±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

11.14±0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Flame Over Circle (GHS03)
GHS07,GHS03
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H272
[Precautionary statements ]

P501-P220-P210-P221-P264-P280-P302+P352-P370+P378-P337+P313-P305+P351+P338-P362+P364-P332+P313
Hazard InformationBack Directory
[Uses]

3-Oxo-1,4-piperidinedicarboxylic Acid 1-(1,1-Dimethylethyl) 4-Methyl Ester is used as a reagent in the synthesis of fused pyrimidines as histamine H4 receptor antagonists. 3-Oxo-1,4-piperidinedicarboxylic Acid 1-(1,1-Dimethylethyl) 4-Methyl Ester is also used as a reagent in the synthesis of heterocycles containing a 4-substituted pyrimidine subunit for pharmaceutical use as mGluR1 antagonists for treatment of migraine.
Spectrum DetailBack Directory
[Spectrum Detail]

Methyl N-Boc-3-Oxopiperidine-4-carboxylate(220223-46-1)1HNMR
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