N1-FMOC- 4-(1-BUT-3-ENOYL)PIPERAZINE - Names and Identifiers
Name | 1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethyl ester
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Synonyms | N1-FMOC- 4-(1-BUT-3-ENOYL)PIPERAZINE 4-(1-BUT-3-ENOYL)PIPERAZINE, N1-FMOC PROTECTED 9H-fluoren-9-ylmethyl 4-but-3-enoylpiperazine-1-carboxylate (9H-Fluoren-9-yl)methyl 4-(but-3-enoyl)piperazine-1-carboxylate [4-(but-3-enoyl)-9H-fluoren-9-yl]Methyl piperazine-1-carboxylate 1-Piperazinecarboxylic acid,4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9 9H-FLUOREN-9-YLMETHYL 4-(3-BUTENOYL)TETRAHYDRO-1(2H)-PYRAZINECARBOXYLATE 1-Piperazinecarboxylicacid,4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethylester 1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethyl ester
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CAS | 876728-43-7
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InChI | InChI=1/C23H24N2O3/c1-2-7-22(26)24-12-14-25(15-13-24)23(27)28-16-21-19-10-5-3-8-17(19)18-9-4-6-11-20(18)21/h2-6,8-11,21H,1,7,12-16H2 |
N1-FMOC- 4-(1-BUT-3-ENOYL)PIPERAZINE - Physico-chemical Properties
Molecular Formula | C23H24N2O3
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Molar Mass | 376.45 |
Density | 1.214g/cm3 |
Melting Point | 105 °C |
Boling Point | 573.2°C at 760 mmHg |
Flash Point | 300.5°C |
Vapor Presure | 3.8E-13mmHg at 25°C |
Storage Condition | 2-8°C |
Refractive Index | 1.603 |
N1-FMOC- 4-(1-BUT-3-ENOYL)PIPERAZINE - Introduction
1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethyl ester is an organic compound, also known as 1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-, 9H-fluoren-9-methylethyl ester.
Nature:
-Appearance: White solid
-Molecular formula: C26H26N2O3
-Molecular weight: 414.5g/mol
-Melting point: 104-106°C
-Boiling point: 563.1°C
-Solubility: Soluble in ethanol, dimethylformamide and chloroform
Use:
- 1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethyl ester can be used in the field of organic synthesis and has potential application value in the pharmaceutical and pesticide industries.
-It is also used as a precursor substance for dyes and pigments.
Preparation Method:
The synthesis of-1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethyl ester requires a series of organic synthesis steps. For example, this compound can be obtained by reacting piperazine with 4-bromobutenate and then with 3-buten-1-ol.
Safety Information:
The safety of-1-Piperazinecarboxylic acid, 4-(1-oxo-3-buten-1-yl)-,9H-fluoren-9-ylmethyl ester has not been fully evaluated, so appropriate protective measures should be taken when handling and using.
Last Update:2024-04-10 22:29:15