388077-74-5 - Names and Identifiers
Name | 1-Piperidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester
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Synonyms | N-Boc-2-Piperidinecarboxamide N-Boc-2-piperidinecarboxamide 1-Boc-piperidine-2-carboxamide 1-N-Boc-2-piperidinecarboxamide N-BOC-DL-2-PIPERIDINECARBOXAMIDE 1-N-Boc-piperidine-2-carboxamide N-BOC-pipecolinamide, BOC-Pip-NH2 tert-butyl 2-carbamoylpiperidine-1-carboxylate TERT-BUTYL 2-CARBAMOYLPIPERIDINE-1-CARBOXYLATE 2-CARBAMOYL-PIPERIDINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER 1-Piperidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester
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CAS | 388077-74-5
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InChI | InChI=1/C11H20N2O3/c1-11(2,3)16-10(15)13-9(14)8-6-4-5-7-12-8/h8,12H,4-7H2,1-3H3,(H,13,14,15) |
388077-74-5 - Physico-chemical Properties
Molecular Formula | C11H20N2O3
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Molar Mass | 228.29 |
Storage Condition | Sealed in dry,Room Temperature |
Refractive Index | 1.472 |
388077-74-5 - Introduction
1-Piperidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester is an organic compound with the chemical formula C13H23N3O3. It is a solid and can exist as white crystals or crystalline powder.
1-Piperidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester is commonly used as an intermediate in organic synthesis. It can be used to synthesize various drugs and pesticides, especially in the synthesis of blocks and small molecule drugs. In addition, it can also be used as a raw material for light-hardening materials, preservatives, surfactants, and the like.
The method for preparing 1-Piperidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester is usually obtained by the reaction of di-tert-butyl carbonate and 2-piperidinecarboxylic acid chloride. This reaction is generally carried out under an inert gas atmosphere and is relatively slow, requiring a certain time for the reaction.
Regarding safety information, 1-Piperidinecarboxylic acid, 2-(aminocarbonyl)-, 1,1-dimethylethyl ester should be careful to avoid inhalation of gas, dust and skin contact during operation. Wear suitable protective clothing, protective gloves and glasses. During storage, it should be kept isolated from oxidants, strong bases and strong acids. If an accident occurs, it should be handled and cleaned in time to avoid damage to the human body and the environment. When using and handling this compound, please refer to the relevant safety instructions.
Last Update:2024-04-09 20:52:54