Substance
ID:342473
Names and Identifiers
IUPAC name
ethyl piperidine-4-carboxylate
IUPAC Traditional name
ethyl piperidine-4-carboxylate
Synonyms
Ethyl 4-piperidinecarboxylatePiperidin-4-carboxylic acid ethyl ester4-哌啶甲酸乙酯Ethyl isonipecotate异哌啶酸乙酯
Registration numbers
CAS Number
MDL Number
PubChem SID
Beilstein Number
EC Number
Properties
Physical Property
Flash Point
176 °F
80 °C
Boiling Point
204 °C(lit.)
Refractive Index
n20/D 1.459(lit.)
Density
1.02 g/mL at 25 °C(lit.)
Product Information
Empirical Formula (Hill Notation)
C8H15NO2
Purity
98%
Safety Information
Personal Protective Equipment
Eyeshields, Gloves, half-mask respirator (US), multi-purpose combination respirator cartridge (US)
MSDS Link
German water hazard class
3
Molecule Details
Packaging
25, 100 g in glass bottle
Application
Reactant for synthesis of:
• SMN protein modulators1
• β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition2
• Nitroethylenediamines by nucleophilic ring opening of nitroimidazolidinone3
• RhoA inhibitors for cardiovascular disease therapy4
• Saccharin derived Mannich bases as antimicrobials and antioxidants5Reactant for one-pot reductive amination and Suzuki-Miyaura cross coupling of formyl aryl and heteroaryl MIDA boronates6
25, 100 g in glass bottle
Application
Reactant for synthesis of:
• SMN protein modulators1
• β-aryl and β-amino-substituted aliphatic esters by rhodium catalyzed tandem double bond migration/conjugate addition2
• Nitroethylenediamines by nucleophilic ring opening of nitroimidazolidinone3
• RhoA inhibitors for cardiovascular disease therapy4
• Saccharin derived Mannich bases as antimicrobials and antioxidants5Reactant for one-pot reductive amination and Suzuki-Miyaura cross coupling of formyl aryl and heteroaryl MIDA boronates6
Molecular Spectra
No Data Available
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References
No Data Available
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