173774-48-6
(R)-1-N-Boc-4-N-Boc-Piperazine-2-Carboxylic Acid
CAS: 173774-48-6
Molecular Formula: C15H26N2O6
173774-48-6 - Names and Identifiers
| Name | (R)-1-N-Boc-4-N-Boc-Piperazine-2-Carboxylic Acid |
| Synonyms | (R)-1-N-Boc-4-N-Boc-Piperazine-2-Carboxylic Acid (R)-1-N-BOC-4-N-BOC-PIPERAZINE-2-CARBOXYLIC ACID (2R)-1,4-bis(tert-butoxycarbonyl)piperazine-2-carboxylic acid (2R)-1,2,4-Piperazinetricarboxylic acid 1,4-Bis(1,1-Dimethylethyl) Ester 1,2,4-Piperazinetricarboxylic acid, 1,4-bis(1,1-diMethylethyl) ester, (2R)- (2R)-1,4-bis[(2-methylpropan-2-yl)oxy-oxomethyl]-2-piperazinecarboxylic acid |
| CAS | 173774-48-6 |
| InChI | InChI=1/C15H26N2O6/c1-14(2,3)22-12(20)16-7-8-17(10(9-16)11(18)19)13(21)23-15(4,5)6/h10H,7-9H2,1-6H3,(H,18,19)/t10-/m1/s1 |
173774-48-6 - Physico-chemical Properties
| Molecular Formula | C15H26N2O6 |
| Molar Mass | 330.38 |
| Density | 1.200±0.06 g/cm3(Predicted) |
| Boling Point | 443.9±40.0 °C(Predicted) |
| pKa | 3.70±0.20(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.503 |
| Use | This product is for scientific research only and shall not be used for other purposes. |
173774-48-6 - Introduction
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is an organic compound with the formula C16H26N2O5. The following is an introduction to its nature, use, preparation and safety information:
Nature:
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is a white solid with low solubility. It is an acidic compound that can react with bases to form salts. It can react under oxidative conditions and therefore needs to be stored and handled in the absence of oxygen.
Use:
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is an important intermediate compound commonly used in organic synthesis. It can be used to prepare compounds such as pharmaceuticals and pesticides. In addition, it can also be used as a ligand for the catalyst.
Method:
The preparation method of (R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is more complicated, and a multi-step synthesis method is usually used. A commonly used synthetic route is from piperazine, through a multi-step reaction, including substitution, protection, deprotection and esterification steps, and finally get the target compound.
Safety Information:
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is relatively stable under normal operating conditions, but it is an organic compound and is potentially dangerous. Laboratory safe practices should be followed for handling and handling of such compounds. Special care should be taken to avoid contact with oxidizing agents to prevent reaction. At the same time, the inhalation of its dust or vapor should be avoided, and protective equipment such as gloves, glasses and protective covers should be provided if necessary. During storage and handling, it should be sealed and kept away from high temperatures and open flames. During the operation, pay attention to avoid contact with skin and eyes, and pay attention to good ventilation conditions. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
Nature:
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is a white solid with low solubility. It is an acidic compound that can react with bases to form salts. It can react under oxidative conditions and therefore needs to be stored and handled in the absence of oxygen.
Use:
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is an important intermediate compound commonly used in organic synthesis. It can be used to prepare compounds such as pharmaceuticals and pesticides. In addition, it can also be used as a ligand for the catalyst.
Method:
The preparation method of (R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is more complicated, and a multi-step synthesis method is usually used. A commonly used synthetic route is from piperazine, through a multi-step reaction, including substitution, protection, deprotection and esterification steps, and finally get the target compound.
Safety Information:
(R)-1-n-boc-4-n-boc-piperazine-2-carboxylic acid is relatively stable under normal operating conditions, but it is an organic compound and is potentially dangerous. Laboratory safe practices should be followed for handling and handling of such compounds. Special care should be taken to avoid contact with oxidizing agents to prevent reaction. At the same time, the inhalation of its dust or vapor should be avoided, and protective equipment such as gloves, glasses and protective covers should be provided if necessary. During storage and handling, it should be sealed and kept away from high temperatures and open flames. During the operation, pay attention to avoid contact with skin and eyes, and pay attention to good ventilation conditions. In case of accidental contact, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 21:11:58
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View History
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144644-00-8
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243666-13-9