TIMTEC-BB SBB004239
3-Piperidinecarboxamide
CAS: 4138-26-5
Molecular Formula: C6H12N2O
TIMTEC-BB SBB004239 - Names and Identifiers
| Name | 3-Piperidinecarboxamide |
| Synonyms | NIPECOTAMIDE Nipecotamide TIMTEC-BB SBB004239 nipecotic acid amide HEXAHYDRONICOTINAMIDE 3-Piperidinecarboxamide 3-PIPERIDINECARBOXAMIDE 3-Piperdine carboxamide piperidine-3-carboxamide PIPERIDINE-3-CARBOXAMIDE (3R)-3-carbamoylpiperidinium (3S)-3-carbamoylpiperidinium (3R)-piperidine-3-carboxamide |
| CAS | 4138-26-5 |
| EINECS | 223-962-5 |
| InChI | InChI=1/C6H12N2O/c7-6(9)5-2-1-3-8-4-5/h5,8H,1-4H2,(H2,7,9)/p+1/t5-/m0/s1 |
TIMTEC-BB SBB004239 - Physico-chemical Properties
| Molecular Formula | C6H12N2O |
| Molar Mass | 128.17 |
| Density | 1.0754 (rough estimate) |
| Melting Point | 103-106°C(lit.) |
| Boling Point | 237.61°C (rough estimate) |
| Flash Point | 142.3°C |
| Vapor Presure | 0.000553mmHg at 25°C |
| Appearance | White very light reddish yellow powder |
| Color | Yellow |
| pKa | 16.50±0.20(Predicted) |
| Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
| Refractive Index | 1.4880 (estimate) |
| MDL | MFCD00005993 |
| Use | This product is for scientific research only and shall not be used for other purposes. |
TIMTEC-BB SBB004239 - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | 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 | 29339900 |
TIMTEC-BB SBB004239 - Introduction
3-Piperidinecarboxamide is an organic compound with the formula C8H15N3O.
Properties: 3-Piperidinecarboxamide is a solid, often white crystalline. It is easily soluble in water and organic solvents at room temperature. The compound has a neutral pH and can form a stable molecular structure in solution.
Purpose: 3-Piperidinecarboxamide is commonly used as an intermediate to connect different functional groups in chemical synthesis. It also has certain applications in the field of medicine, and can be used to synthesize certain pharmaceutical compounds, such as anti-cancer drugs and antiviral drugs.
Preparation method: A common preparation method is to obtain 3-Piperidinecarboxamide by reacting piperidinecarboxamide chloride with ammonia. Specifically, piperidinecarboxamide is reacted with ammonia in an organic solvent to produce 3-Piperidinecarboxamide and to form the hydrochloride salt.
Safety Information: 3-Piperidinecarboxamide is generally considered to be a relatively safe compound. However, as with any chemical substance, proper handling and handling is important and proper safety measures should be taken. When using this compound, avoid contact with skin and eyes, and ensure a well-ventilated laboratory environment. In the event of accidental contact or misuse, medical help should be sought immediately.
Properties: 3-Piperidinecarboxamide is a solid, often white crystalline. It is easily soluble in water and organic solvents at room temperature. The compound has a neutral pH and can form a stable molecular structure in solution.
Purpose: 3-Piperidinecarboxamide is commonly used as an intermediate to connect different functional groups in chemical synthesis. It also has certain applications in the field of medicine, and can be used to synthesize certain pharmaceutical compounds, such as anti-cancer drugs and antiviral drugs.
Preparation method: A common preparation method is to obtain 3-Piperidinecarboxamide by reacting piperidinecarboxamide chloride with ammonia. Specifically, piperidinecarboxamide is reacted with ammonia in an organic solvent to produce 3-Piperidinecarboxamide and to form the hydrochloride salt.
Safety Information: 3-Piperidinecarboxamide is generally considered to be a relatively safe compound. However, as with any chemical substance, proper handling and handling is important and proper safety measures should be taken. When using this compound, avoid contact with skin and eyes, and ensure a well-ventilated laboratory environment. In the event of accidental contact or misuse, medical help should be sought immediately.
Last Update：2024-04-09 20:45:29
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