Benzyl 4-(aminocarbonyl)piperidine-1-carboxylate - Names and Identifiers
Benzyl 4-(aminocarbonyl)piperidine-1-carboxylate - Physico-chemical Properties
Molecular Formula | C14H18N2O3
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Molar Mass | 262.3 |
Density | 1.224±0.06 g/cm3(Predicted) |
Melting Point | 130 °C |
Boling Point | 475.5±44.0 °C(Predicted) |
Flash Point | 241.4°C |
Vapor Presure | 3.3E-09mmHg at 25°C |
pKa | 16.40±0.20(Predicted) |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.568 |
MDL | MFCD01568760 |
Benzyl 4-(aminocarbonyl)piperidine-1-carboxylate - Risk and Safety
Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin.
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Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection.
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Benzyl 4-(aminocarbonyl)piperidine-1-carboxylate - Introduction
BENZYL 4-(AMINOCARBONYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE is an organic compound with the chemical formula C19H19N3O2. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: BENZYL 4-(AMINOCARBONYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE is a white to yellowish solid.
-Solubility: It can be dissolved in some organic solvents (such as dimethylformamide and chloroform), but its solubility in water is low.
-Melting Point: its melting point is about 140-145 ℃.
Use:
- BENZYL 4-(AMINOCARBONYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE has certain applications in the field of medicinal chemistry. It can be used as an intermediate in the synthesis of bioactive molecules for the preparation of anti-tumor and anti-infection drugs.
-It can also be used as a protecting group (protecting hydroxyl group) or activating agent in organic synthesis.
Method:
The preparation of-BENZYL 4-(AMINOCARBONYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE can be obtained by reacting piperidine with formyl chloride. First, piperidine is Ketal with formic acid under basic conditions to form an N-formylated intermediate, which is then chlorinated with thionyl chloride to form the ring at the C4 position. Finally, this intermediate was reacted with BENZYL benzoate to give BENZYL 4-(AMINOCARBONYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE.
Safety Information:
- BENZYL 4-(AMINOCARBONYL)TETRAHYDRO-1(2H)-PYRIDINECARBOXYLATE has no obvious toxicity or danger under normal use conditions.
-But in the process of operation, still need to pay attention to the following matters:
-Avoid contact with skin and wear suitable protective gloves, goggles, etc.
-avoid inhalation of its dust or steam, the use of the need to maintain good ventilation conditions.
-Do not eat or drink during operation, and avoid eating by mistake.
-Follow proper laboratory procedures and personal protective measures when using or handling the compound.
Last Update:2024-04-09 21:01:54