Molecular Formula | C13H15NO3 |
Molar Mass | 233.26 |
Density | 1.172 g/mL at 25 °C (lit.) |
Melting Point | 38-41°C |
Boling Point | 114-140 °C/0.25 mmHg (lit.) |
Flash Point | >110 °C |
Solubility | Chloroform, Dichloromethane, Ethyl Acetate, Methanol |
Vapor Presure | 4.18E-06mmHg at 25°C |
Appearance | White solid |
Specific Gravity | 1.185 |
Color | White to pale yellow or clear |
BRN | 1533716 |
pKa | -1.63±0.20(Predicted) |
Storage Condition | Sealed in dry,2-8°C |
Refractive Index | n20/D 1.542(lit.) |
MDL | MFCD00673144 |
Physical and Chemical Properties | WGK Germany:3 |
Use | Protective piperidone can carry out synthetic conversion reactions that have attracted much attention, including Knoevenagel reactions, heterogeneous Diels-Alder reactions, and reactions to generate N-(4-piperidinyl) hydroxyindole. The raw material for the synthesis of GABA analogs by direct Barbier-type addition reaction of alkyl phosphinates. |
Hazard Symbols | Xi - Irritant |
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. S36 - Wear suitable protective clothing. S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S37/39 - Wear suitable gloves and eye/face protection |
WGK Germany | 3 |
HS Code | 29333990 |
Use | Protective piperidone can be used for synthetic conversion reactions that have attracted much attention, including Knoevenagel reactions, Heterogeneous Diels-Alder reaction and reaction to generate N-(4-piperidinyl) hydroxy indole. The raw material for the synthesis of GABA analogs by direct Barbier-type addition reaction of alkyl phosphinates. |