tert-Butyl 4-(3-aminopropyl)piperazine-1-carboxylate
tert-butyl 4-(3-aminopropyl)piperazine-1-carboxylate
CAS: 373608-48-1
Molecular Formula: C12H25N3O2
tert-Butyl 4-(3-aminopropyl)piperazine-1-carboxylate - Names and Identifiers
tert-Butyl 4-(3-aminopropyl)piperazine-1-carboxylate - Physico-chemical Properties
| Molecular Formula | C12H25N3O2 |
| Molar Mass | 243.35 |
| Density | 1.042±0.06 g/cm3 (20 ºC 760 Torr) |
| Boling Point | 339.6±37.0 °C(Predicted) |
| Flash Point | 159.2°C |
| Vapor Presure | 9.1E-05mmHg at 25°C |
| pKa | 10.39±0.10(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
| Refractive Index | 1.493 |
tert-Butyl 4-(3-aminopropyl)piperazine-1-carboxylate - Risk and Safety
| Hazard Class | IRRITANT |
tert-Butyl 4-(3-aminopropyl)piperazine-1-carboxylate - Introduction
tert-butyl 4-(3-aminopropyl)piperazine-1-carboxylate is an organic compound. Its chemical formula is C14H28N2O2. The following is a description of the properties, uses, preparation and safety information of this compound:
Nature:
-Appearance: White crystal or crystalline powder
-melting point: about 45-50 ℃
-Solubility: Soluble in some organic solvents, such as ethanol and chloroform
Use:
tert-butyl 4-(3-aminoppyl) piperazine-1-carboxylate is mainly used in the field of medicine, as a pharmaceutical intermediate. It can be used in the synthesis of bioactive compounds, such as anti-tumor drugs, antidepressants, etc., with a wide range of applications.
Preparation Method:
tert-butyl 4-(3-aminoppyl) piperazine-1-carboxylate can be prepared by the following steps:
1. tert-butyl alcohol is reacted with 4-piperazine methylamine to generate tert-butyl -4-piperazine methanol.
2. Preparation of 3-aminopropionaldehyde.
3. reacting 3-aminopropionaldehyde with tert-butyl-4-piperazine methanol to generate the tert-butyl 4-(3-aminopropyl)piperazine-1-carboxylate.
Safety Information:
-Harm to human body: Although there is no detailed toxicity study report for this compound, in general, safe operating procedures should be followed during use. Direct contact may cause irritation and allergic reactions.
-Environmental impact: The impact of this compound in the environment has not been studied in detail, but it should be handled and disposed of in accordance with the principles of environmental protection.
Please note that the use of this compound should follow appropriate operating procedures to ensure personal safety and safety of the experimental environment. This information is for reference only, please refer to the relevant chemical literature and laboratory practices for specific use.
Nature:
-Appearance: White crystal or crystalline powder
-melting point: about 45-50 ℃
-Solubility: Soluble in some organic solvents, such as ethanol and chloroform
Use:
tert-butyl 4-(3-aminoppyl) piperazine-1-carboxylate is mainly used in the field of medicine, as a pharmaceutical intermediate. It can be used in the synthesis of bioactive compounds, such as anti-tumor drugs, antidepressants, etc., with a wide range of applications.
Preparation Method:
tert-butyl 4-(3-aminoppyl) piperazine-1-carboxylate can be prepared by the following steps:
1. tert-butyl alcohol is reacted with 4-piperazine methylamine to generate tert-butyl -4-piperazine methanol.
2. Preparation of 3-aminopropionaldehyde.
3. reacting 3-aminopropionaldehyde with tert-butyl-4-piperazine methanol to generate the tert-butyl 4-(3-aminopropyl)piperazine-1-carboxylate.
Safety Information:
-Harm to human body: Although there is no detailed toxicity study report for this compound, in general, safe operating procedures should be followed during use. Direct contact may cause irritation and allergic reactions.
-Environmental impact: The impact of this compound in the environment has not been studied in detail, but it should be handled and disposed of in accordance with the principles of environmental protection.
Please note that the use of this compound should follow appropriate operating procedures to ensure personal safety and safety of the experimental environment. This information is for reference only, please refer to the relevant chemical literature and laboratory practices for specific use.
Last Update：2024-04-09 15:17:57
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CAS: 373608-48-1
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View History
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