N,N-dimethylpiperidin-3-amine
N,N-dimethylpiperidin-3-amine
CAS: 50534-49-1
Molecular Formula: C7H16N2
N,N-dimethylpiperidin-3-amine - Names and Identifiers
| Name | N,N-dimethylpiperidin-3-amine |
| Synonyms | CHEMBRDG-BB 4018212 DIMETHYLAMINOPIPERIDINE 3-DIMETHYLAMINOPIPERIDINE N,N-dimethylpiperidin-3-amine N,N-Dimethylpiperidin-3-amine DiMethyl-piperidin-3-yl-aMine N,N-DIMETHYLPIPERIDIN-3-AMINE 3-PiperidinaMine,N,N-diMethyl- 3-Piperidinamine, N,N-dimethyl- |
| CAS | 50534-49-1 |
| InChI | InChI=1/C7H16N2/c1-9(2)7-4-3-5-8-6-7/h7-8H,3-6H2,1-2H3 |
N,N-dimethylpiperidin-3-amine - Physico-chemical Properties
| Molecular Formula | C7H16N2 |
| Molar Mass | 128.22 |
| Density | 0.91±0.1 g/cm3(Predicted) |
| Boling Point | 58°C/7mm |
| Flash Point | 65.171°C |
| Vapor Presure | 0.836mmHg at 25°C |
| pKa | 9.83±0.10(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
| Refractive Index | 1.479 |
N,N-dimethylpiperidin-3-amine - Introduction
N,N-dimethylpiperidin-3-amine is an organic compound with the chemical formula C8H18N2. It is a colorless or pale yellow liquid with a strong ammonia odor.
N,N-dimethylpiperidin-3-amine has a wide range of applications in the field of pharmaceutical synthesis and organic synthesis. It is commonly used as ammonia source and alkali catalyst in organic synthesis, and can participate in acylation, acetylation, aminoalkylation and other reactions.
The common method for the preparation of N,N-dimethylpiperidin-3-amine is obtained by the reaction of methylpiperidine and dimethylamine. The specific preparation process may be that methylpiperidine is mixed with dimethylamine in a molar ratio of 1:1, and the reaction is carried out at an appropriate temperature and pressure, usually under the protection of a solvent catalyst and an inert gas.
Regarding the safety information of N,N-dimethylpiperidin-3-amine, it is a corrosive substance that can cause irritation and irritation in contact with skin and eyes
N,N-dimethylpiperidin-3-amine has a wide range of applications in the field of pharmaceutical synthesis and organic synthesis. It is commonly used as ammonia source and alkali catalyst in organic synthesis, and can participate in acylation, acetylation, aminoalkylation and other reactions.
The common method for the preparation of N,N-dimethylpiperidin-3-amine is obtained by the reaction of methylpiperidine and dimethylamine. The specific preparation process may be that methylpiperidine is mixed with dimethylamine in a molar ratio of 1:1, and the reaction is carried out at an appropriate temperature and pressure, usually under the protection of a solvent catalyst and an inert gas.
Regarding the safety information of N,N-dimethylpiperidin-3-amine, it is a corrosive substance that can cause irritation and irritation in contact with skin and eyes
Last Update：2024-04-09 21:54:55
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View History
N,N-dimethylpiperidin-3-amine
水合氯醛
5-Cyclodecen-1-one,2-ethoxy-6-methyl-,(E)-(9CI)
氟化乙烯
4-BROMOTHIOPHENE-2-CARBALDEHYDE
1-benzylpyridinium-3-carboxylate
水合氯醛
5-Cyclodecen-1-one,2-ethoxy-6-methyl-,(E)-(9CI)
氟化乙烯
4-BROMOTHIOPHENE-2-CARBALDEHYDE
1-benzylpyridinium-3-carboxylate