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4-Aminomethyl-1-Boc-piperidine, 97%, Thermo Scientific Chemicals
1675.00 NOK - 6155.00 NOK
Chemical Identifiers
CAS | 144222-22-0 |
---|---|
Molecular Formula | C11H23N2O2 |
Molecular Weight (g/mol) | 215.32 |
MDL Number | MFCD01076207 |
InChI Key | KLKBCNDBOVRQIJ-UHFFFAOYSA-O |
Synonym | 1-boc-4-aminomethyl piperidine, tert-butyl 4-aminomethyl piperidine-1-carboxylate, 1-boc-4-aminomethylpiperidine, 1-boc-4-aminomethyl-piperidine, 4-aminomethyl-1-n-boc-piperidine, boc-4-aminomethyl-piperidine, 4-aminomethyl-1-n-t-butoxycarbonyl piperidine, 4-aminomethyl-1-boc-piperidine, 1-n-boc-4-aminomethyl piperidine, 4-aminomethyl-piperidine-1-carboxylic acid tert-butyl esterShow More |
PubChem CID | 736817 |
IUPAC Name | {1-[(tert-butoxy)carbonyl]piperidin-4-yl}methanaminium |
SMILES | CC(C)(C)OC(=O)N1CCC(C[NH3+])CC1 |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
---|---|---|---|---|---|---|---|---|---|
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
15409587
|
Thermo Scientific Alfa Aesar
H52819.06 |
5 g |
1675.00 NOK
5g |
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15419587
|
Thermo Scientific Alfa Aesar
H52819.14 |
25 g |
6155.00 NOK
25g |
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Description
4-Aminomethyl-1-Boc-piperidine is used in the preparation biologically active compounds and orally active platelet-activating factor antagonists. It is used as an inhibitor for aspartic acid protease and Kinesin spindle protein. It is an active reactant involved in the enantioselective synthesis of N-alkyl terminal aziridines.
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-Aminomethyl-1-Boc-piperidine is used in the preparation biologically active compounds and orally active platelet-activating factor antagonists. It is used as an inhibitor for aspartic acid protease and Kinesin spindle protein. It is an active reactant involved in the enantioselective synthesis of N-alkyl terminal aziridines.
Solubility
Soluble in chloroform and methanol.
Notes
Store in a cool place. Keep the container tightly closed in a dry and well-ventilated place. Incompatible with strong oxidizing agents.
Chemical Identifiers
144222-22-0 | |
215.32 | |
KLKBCNDBOVRQIJ-UHFFFAOYSA-O | |
736817 | |
CC(C)(C)OC(=O)N1CCC(C[NH3+])CC1 |
C11H23N2O2 | |
MFCD01076207 | |
1-boc-4-aminomethyl piperidine, tert-butyl 4-aminomethyl piperidine-1-carboxylate, 1-boc-4-aminomethylpiperidine, 1-boc-4-aminomethyl-piperidine, 4-aminomethyl-1-n-boc-piperidine, boc-4-aminomethyl-piperidine, 4-aminomethyl-1-n-t-butoxycarbonyl piperidine, 4-aminomethyl-1-boc-piperidine, 1-n-boc-4-aminomethyl piperidine, 4-aminomethyl-piperidine-1-carboxylic acid tert-butyl esterShow More | |
{1-[(tert-butoxy)carbonyl]piperidin-4-yl}methanaminium |
Specifications
144222-22-0 | |
237°C to 238°C | |
C11H23N2O2 | |
1-boc-4-aminomethyl piperidine, tert-butyl 4-aminomethyl piperidine-1-carboxylate, 1-boc-4-aminomethylpiperidine, 1-boc-4-aminomethyl-piperidine, 4-aminomethyl-1-n-boc-piperidine, boc-4-aminomethyl-piperidine, 4-aminomethyl-1-n-t-butoxycarbonyl piperidine, 4-aminomethyl-1-boc-piperidine, 1-n-boc-4-aminomethyl piperidine, 4-aminomethyl-piperidine-1-carboxylic acid tert-butyl ester | |
KLKBCNDBOVRQIJ-UHFFFAOYSA-O | |
{1-[(tert-butoxy)carbonyl]piperidin-4-yl}methanaminium | |
736817 | |
97% |
1.013 | |
>110°C (230°F) | |
MFCD01076207 | |
Soluble in chloroform and methanol. | |
CC(C)(C)OC(=O)N1CCC(C[NH3+])CC1 | |
215.32 | |
214.31 | |
4-Aminomethyl-1-Boc-piperidine |
Safety and Handling
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P260-P264b-P271-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P501c
H314-H335
missing translation for 'dotInformation' : Hazard Class: 8; Packaging Group: III
missing translation for 'tsca' : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only
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