1-N-Boc-4-(Phenylamino)piperidine
- CAS No.
- 125541-22-2
- Chemical Name:
- 1-N-Boc-4-(Phenylamino)piperidine
- Synonyms
- tert-butyl 4-anilinopiperidine-1-carboxylate;1-Boc-4-(phenylaMino)piperidine;tert-butyl 4-(phenylaMino)piperidine-1-carboxylate;1-N-Boc-4-(Phenylamino);Aniline piperidine;(Phenylamino)piperidine;4-(Phenylamino)piperidine, N1-BOC protected;2-Methyl-2-propanyl 4-anilino-1-piperidinecarboxylate;4-(phenylamino)-;1-N-Boc-4-(Phenylami
- CBNumber:
- CB2262675
- Molecular Formula:
- C16H24N2O2
- Molecular Weight:
- 276.37
- MDL Number:
- MFCD02102489
- MOL File:
- 125541-22-2.mol
| Melting point | 136-137 |
|---|---|
| Boiling point | 400.6±38.0 °C(Predicted) |
| Density | 1.107±0.06 g/cm3(Predicted) |
| storage temp. | Keep in dark place,Inert atmosphere,Room temperature |
| solubility | DMF: 15mg/mL; DMSO: 25mg/mL; Ethanol: 25mg/mL; Ethanol:PBS (pH 7.2) (1:1): 0.5mg/mL |
| form | A crystalline solid |
| pka | 5.00±0.20(Predicted) |
| InChI | InChI=1S/C16H24N2O2/c1-16(2,3)20-15(19)18-11-9-14(10-12-18)17-13-7-5-4-6-8-13/h4-8,14,17H,9-12H2,1-3H3 |
| InChIKey | HTIWISWAPVQGMI-UHFFFAOYSA-N |
| SMILES | N1(C(OC(C)(C)C)=O)CCC(NC2=CC=CC=C2)CC1 |
| FDA UNII | 5PB6P54SRS |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Warning | |||||||||
| Hazard statements | H315-H319-H335 | |||||||||
| Precautionary statements | P261-P305+P351+P338 | |||||||||
| Hazard Codes | Xi,Xn | |||||||||
| Risk Statements | 22 | |||||||||
| Hazard Note | Harmful/Irritant | |||||||||
| HazardClass | IRRITANT | |||||||||
| HS Code | 2933399990 | |||||||||
| NFPA 704 |
|
1-N-Boc-4-(Phenylamino)piperidine Chemical Properties,Uses,Production
Description
4-Anilino-1-Boc-piperidine is an analytical reference standard that is structurally similar to known opioids. 4-Anilino-1-Boc-piperidine is a precursor in the synthesis of 4-anilinopiperidine . This product is intended for research and forensic applications.
Chemical Properties
Pale Brown Solid
Uses
Intermediate in the preparation of Fentanyl derivatives.
Application
1-N-Boc-4-(Phenylamino)piperidine is an amino acid derivative widely employed as a reagent in organic synthesis. This compound exhibits remarkable versatility, finding applications in various fields such as peptide and protein synthesis, organic synthesis, and drug development. It possesses strong basic properties, allowing for diverse reactions with acids that lead to the formation of a wide array of products. The extensive use of this compound in organic synthesis is well-documented, particularly in the synthesis of peptides and proteins. By facilitating the coupling of amino acids, it enables the creation of peptides that can be utilized in diverse applications, including the development of pharmaceutical drugs.
1-N-Boc-4-(Phenylamino)piperidine Preparation Products And Raw materials
Raw materials
Preparation Products
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