124932-43-0
(R)-3-Aminohexahydroazepine
CAS: 124932-43-0
Molecular Formula: C6H14N2
124932-43-0 - Names and Identifiers
124932-43-0 - Physico-chemical Properties
| Molecular Formula | C6H14N2 |
| Molar Mass | 114.19 |
| Density | 0.893 |
| Boling Point | 180.9℃ |
| Flash Point | 69.6℃ |
| pKa | 10.66±0.40(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
| Use | This product is for scientific research only and shall not be used for other purposes. |
124932-43-0 - Introduction
(R)-3-Aminohexaazepine, also known as (R)-3-aminothiazole [1,5-a]= [1,3,5] triazacyclohexane, is an organic compound. Its chemical formula is C3H8N4S.
(R)-3-Aminohexaazepine is a chiral molecule with optical rotation. Its optical activity will lead to different interactions with other chiral compounds.
(R)-3-amino-hexahydroazepine has some applications in the field of medicine. It is a potential drug candidate for the treatment of Parkinson's disease. It can reduce the symptoms of Parkinson's disease by regulating the level of dopamine in the brain.
The preparation of (R)-3-aminohexahydroazepine can be achieved by chemical synthesis. A common preparation method is to obtain the target compound by chiral separation of the synthetic precursor compounds.
With regard to the safety information of (R)-3-amino-hexahydroazepine, there has not been sufficient research and evaluation regarding its toxicity and precautions for use. Therefore, it is necessary to follow the routine laboratory safety operation and protective measures during use to protect personal safety.
(R)-3-Aminohexaazepine is a chiral molecule with optical rotation. Its optical activity will lead to different interactions with other chiral compounds.
(R)-3-amino-hexahydroazepine has some applications in the field of medicine. It is a potential drug candidate for the treatment of Parkinson's disease. It can reduce the symptoms of Parkinson's disease by regulating the level of dopamine in the brain.
The preparation of (R)-3-aminohexahydroazepine can be achieved by chemical synthesis. A common preparation method is to obtain the target compound by chiral separation of the synthetic precursor compounds.
With regard to the safety information of (R)-3-amino-hexahydroazepine, there has not been sufficient research and evaluation regarding its toxicity and precautions for use. Therefore, it is necessary to follow the routine laboratory safety operation and protective measures during use to protect personal safety.
Last Update：2024-04-09 21:54:55
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