missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Please login to your online account to display your discounted pricing
4-Amino-1-Boc-piperidine, 97%, Thermo Scientific Chemicals
$107.00 - $321.47
Chemical Identifiers
| CAS | 87120-72-7 |
|---|---|
| Molecular Formula | C10H21N2O2 |
| Molecular Weight (g/mol) | 201.29 |
| MDL Number | MFCD01076201 |
| InChI Key | LZRDHSFPLUWYAX-UHFFFAOYSA-O |
| Synonym | 4-amino-1-boc-piperidine, 1-boc-4-aminopiperidine, n-boc-4-aminopiperidine, n-boc-4-amino-piperidine, 4-amino-1-n-boc-piperidine, 4-amino-n-boc piperidine, 1-boc-4-amino piperidine, 1-n-boc-4-aminopiperidine, 1-t-butoxycarbonyl-4-aminopiperidine, n-1-boc-4-aminopiperidine |
| PubChem CID | 1268291 |
| IUPAC Name | tert-butyl 4-aminopiperidine-1-carboxylate |
| SMILES | CC(C)(C)OC(=O)N1CCC([NH3+])CC1 |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|
AAH3077903
|
Thermo Scientific Chemicals
H3077903 |
1 g |
Each for $107.00
|
|
|||||
|
AAH3077906
|
Thermo Scientific Chemicals
H3077906 |
5 g |
Each for $321.47
|
|
|||||
Description
4-Amino-1-Boc-piperidine is a chemical reagent used in the preparation of pharmaceutical compounds. Used in the synthesis of bromodomain inhibitors as well as HepG2 cell cycle inhibitors used in anti-tumor therapy. Also employed in a microwave-assisted solid-phase synthesis of N-substituted piperidines via direct annulation of primary amines with resin-bound dimesylates.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications4-Amino-1-Boc-piperidine is a chemical reagent used in the preparation of pharmaceutical compounds. Used in the synthesis of bromodomain inhibitors as well as HepG2 cell cycle inhibitors used in anti-tumor therapy. Also employed in a microwave-assisted solid-phase synthesis of N-substituted piperidines via direct annulation of primary amines with resin-bound dimesylates.
Solubility
Insoluble in water.
Notes
Air Sensitive, store away from air. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from oxidizing agent.
Chemical Identifiers
| 87120-72-7 | |
| 201.29 | |
| LZRDHSFPLUWYAX-UHFFFAOYSA-O | |
| 1268291 | |
| CC(C)(C)OC(=O)N1CCC([NH3+])CC1 |
| C10H21N2O2 | |
| MFCD01076201 | |
| 4-amino-1-boc-piperidine, 1-boc-4-aminopiperidine, n-boc-4-aminopiperidine, n-boc-4-amino-piperidine, 4-amino-1-n-boc-piperidine, 4-amino-n-boc piperidine, 1-boc-4-amino piperidine, 1-n-boc-4-aminopiperidine, 1-t-butoxycarbonyl-4-aminopiperidine, n-1-boc-4-aminopiperidine | |
| tert-butyl 4-aminopiperidine-1-carboxylate |
Specifications
| 87120-72-7 | |
| C10H21N2O2 | |
| 1 g | |
| Air Sensitive | |
| Insoluble in water. | |
| CC(C)(C)OC(=O)N1CCC([NH3+])CC1 | |
| 201.29 | |
| 200.28 | |
| 4-Amino-1-Boc-piperidine |
| 44°C to 48°C | |
| MFCD01076201 | |
| UN3259 | |
| 4-amino-1-boc-piperidine, 1-boc-4-aminopiperidine, n-boc-4-aminopiperidine, n-boc-4-amino-piperidine, 4-amino-1-n-boc-piperidine, 4-amino-n-boc piperidine, 1-boc-4-amino piperidine, 1-n-boc-4-aminopiperidine, 1-t-butoxycarbonyl-4-aminopiperidine, n-1-boc-4-aminopiperidine | |
| LZRDHSFPLUWYAX-UHFFFAOYSA-O | |
| tert-butyl 4-aminopiperidine-1-carboxylate | |
| 1268291 | |
| 97% |
Safety and Handling
GHS H Statement
H314-H318
Causes severe skin burns and eye damage.
Causes serious eye damage.
P260-P264b-P270-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P501c
H302-H314
DOTInformation : Transport Hazard Class: 8; Packing Group: III; Proper Shipping Name: AMINES, SOLID, CORROSIVE, N.O.S.
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only