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1-Boc-piperidine-4-carboxaldehyde, 97%
CAS: 137076-22-3 | C11H19NO3 | 213.28 g/mol
$161.88 - $575.49
Identifiants chimiques
| CAS | 137076-22-3 |
|---|---|
| Molecular Formula | C11H19NO3 |
| Molecular Weight (g/mol) | 213.28 |
| MDL Number | MFCD02179019 |
| InChI Key | JYUQEWCJWDGCRX-UHFFFAOYSA-N |
| Synonym | 1-boc-4-piperidinecarboxaldehyde, 1-boc-4-formylpiperidine, 1-tert-butoxycarbonyl-4-piperidinecarboxaldehyde, 1-boc-piperidine-4-carboxaldehyde, n-boc-4-formylpiperidine, n-boc-4-piperidinecarboxaldehyde, 1-tert-butoxycarbonyl-4-formylpiperidine, 4-formyl-piperidine-1-carboxylic acid tert-butyl ester, n-boc-piperidine-4-carbaldehyde, 4-formylpiperidine-1-carboxylic acid tert-butyl ester |
| PubChem CID | 1514430 |
| IUPAC Name | tert-butyl 4-formylpiperidine-1-carboxylate |
| SMILES | CC(C)(C)OC(=O)N1CCC(CC1)C=O |
| Numéro de catalogue | Numéro du manufacturier. | Quantity | Prix | Quantité | |||||
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| Numéro de catalogue | Numéro du manufacturier. | Quantity | Prix | Quantité | |||||
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AAH5281303
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Thermo Scientific Chemicals
H5281303 |
1 g |
chaque for $161.88
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Connectez-vous ou enregistrez-vous pour vérifier votre prix et la disponibilité.
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AAH5281306
|
Thermo Scientific Chemicals
H5281306 |
5 g |
chaque for $575.49
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|
Connectez-vous ou enregistrez-vous pour vérifier votre prix et la disponibilité.
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Description
1-Boc-piperidine-4-carboxaldehyde is used as reactant for synthesis of Pim-1 inhibitors, selective GPR119 agonists for type II diabetes, M-tropic (R5) HIV-1 replication inhibitors, HDAC inhibitors and selective 5-HT6 antagonists. It is also used as reactant for three-component vinylogous Mannich reactions
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.
Applications1-Boc-piperidine-4-carboxaldehyde is used as reactant for synthesis of Pim-1 inhibitors, selective GPR119 agonists for type II diabetes, M-tropic (R5) HIV-1 replication inhibitors, HDAC inhibitors and selective 5-HT6 antagonists. It is also used as reactant for three-component vinylogous Mannich reactions
Solubility
Soluble in methanol.
Notes
Air sensitive. Incompatible with oxidizing agents.
Identifiants chimiques
| 137076-22-3 | |
| 213.28 | |
| JYUQEWCJWDGCRX-UHFFFAOYSA-N | |
| 1514430 | |
| CC(C)(C)OC(=O)N1CCC(CC1)C=O |
| C11H19NO3 | |
| MFCD02179019 | |
| 1-boc-4-piperidinecarboxaldehyde, 1-boc-4-formylpiperidine, 1-tert-butoxycarbonyl-4-piperidinecarboxaldehyde, 1-boc-piperidine-4-carboxaldehyde, n-boc-4-formylpiperidine, n-boc-4-piperidinecarboxaldehyde, 1-tert-butoxycarbonyl-4-formylpiperidine, 4-formyl-piperidine-1-carboxylic acid tert-butyl ester, n-boc-piperidine-4-carbaldehyde, 4-formylpiperidine-1-carboxylic acid tert-butyl ester | |
| tert-butyl 4-formylpiperidine-1-carboxylate |
Spécifications
| 137076-22-3 | |
| MFCD02179019 | |
| Air sensitive | |
| Soluble in methanol. | |
| CC(C)(C)OC(=O)N1CCC(CC1)C=O | |
| 213.28 | |
| 213.28 | |
| 1-Boc-piperidine-4-carboxaldehyde |
| C11H19NO3 | |
| 1 g | |
| 1-boc-4-piperidinecarboxaldehyde, 1-boc-4-formylpiperidine, 1-tert-butoxycarbonyl-4-piperidinecarboxaldehyde, 1-boc-piperidine-4-carboxaldehyde, n-boc-4-formylpiperidine, n-boc-4-piperidinecarboxaldehyde, 1-tert-butoxycarbonyl-4-formylpiperidine, 4-formyl-piperidine-1-carboxylic acid tert-butyl ester, n-boc-piperidine-4-carbaldehyde, 4-formylpiperidine-1-carboxylic acid tert-butyl ester | |
| JYUQEWCJWDGCRX-UHFFFAOYSA-N | |
| tert-butyl 4-formylpiperidine-1-carboxylate | |
| 1514430 | |
| 97% |
Sécurité et manipulation
GHS H Statement
H315-H319-H335
Causes skin irritation.
Causes serious eye irritation.
May cause respiratory irritation.
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
missing translation for 'tsca' : No
Recommended Storage : Keep cold
RUO – Research Use Only