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1-Boc-piperidine-4-carboxaldehyde, 97%, Thermo Scientific Chemicals
36.48 € - 389.94 €
Chemical Identifiers
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 esterShow More |
PubChem CID | 1514430 |
IUPAC Name | tert-butyl 4-formylpiperidine-1-carboxylate |
SMILES | CC(C)(C)OC(=O)N1CCC(CC1)C=O |
Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
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Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
15459577
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Thermo Scientific Alfa Aesar
H52813.MD |
250 mg | N/A | ||||||
15439577
|
Thermo Scientific Alfa Aesar
H52813.03 |
1 g |
109.55 €
1g |
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15449577
|
Thermo Scientific Alfa Aesar
H52813.06 |
5 g |
389.94 €
5g |
Please sign in to purchase this item. Need a web account? Register with us today! | |||||
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.
Chemical Identifiers
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 esterShow More | |
tert-butyl 4-formylpiperidine-1-carboxylate |
Specifications
137076-22-3 | |
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 | |
JYUQEWCJWDGCRX-UHFFFAOYSA-N | |
tert-butyl 4-formylpiperidine-1-carboxylate | |
1514430 | |
97% |
C11H19NO3 | |
Air sensitive | |
Soluble in methanol. | |
CC(C)(C)OC(=O)N1CCC(CC1)C=O | |
213.28 | |
213.28 | |
1-Boc-piperidine-4-carboxaldehyde |
Safety and Handling
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
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