4-Piperidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-α,3-dioxo-, methyl ester
tert-Butyl 4-(2-methoxy-2-oxoacetyl)-3-oxopiperidine-1-carboxylate
CAS: 1159983-63-7
Molecular Formula: C13H19NO6
4-Piperidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-α,3-dioxo-, methyl ester - Names and Identifiers
4-Piperidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-α,3-dioxo-, methyl ester - Physico-chemical Properties
| Molecular Formula | C13H19NO6 |
| Molar Mass | 285.29 |
| Density | 1.227 |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD11111571 |
4-Piperidineacetic acid, 1-[(1,1-dimethylethoxy)carbonyl]-α,3-dioxo-, methyl ester - Introduction
tert-Butyl 4-(2-methoxy-2-oxoacetyl)-3-oxopiperidine-1-carboxylate, also known as tert-butyl alcohol 4-(2-methoxy-2-oxoacetyl)-3-chloropiperidine -1-carboxylate, the chemical formula is C14H21NO6 and the molecular weight is 299.32.
Properties: The compound is a white to light yellow solid. It is non-volatile at room temperature, soluble in organic solvents such as chloroform, ether and dimethyl sulfoxide, and poorly soluble in water.
Purpose: This compound is often used as a reagent in organic synthesis for the synthesis of biologically active compounds, such as drugs and fine chemicals. It has a wide range of applications in the field of medicine, can be used to prepare anti-virus, anti-tumor and anti-inflammatory drugs.
Preparation method: The preparation method of tert-Butyl 4-(2-methoxy-2-oxoacetyl)-3-oxopiperidine-1-carboxylate is relatively complicated and includes multiple steps. First, t-butanol is converted to a carboxylic acid ester compound by a chemical reaction. The carboxylic acid ester is then combined with the piperidine using an appropriate reagent and the methoxy and formyl functional groups are introduced by reaction. Finally, the carboxylic acid ester is converted to the desired compound by oxidation, protection and reaction.
Safety information: tert-Butyl 4-(2-methody-2-oxoacetyl)-3-oxopperidine-1-boxylate has no special safety risk information to report. However, as a chemical substance, it should comply with laboratory safety procedures and avoid direct contact with skin and eyes. If ingested or inhaled, seek medical help immediately.
Properties: The compound is a white to light yellow solid. It is non-volatile at room temperature, soluble in organic solvents such as chloroform, ether and dimethyl sulfoxide, and poorly soluble in water.
Purpose: This compound is often used as a reagent in organic synthesis for the synthesis of biologically active compounds, such as drugs and fine chemicals. It has a wide range of applications in the field of medicine, can be used to prepare anti-virus, anti-tumor and anti-inflammatory drugs.
Preparation method: The preparation method of tert-Butyl 4-(2-methoxy-2-oxoacetyl)-3-oxopiperidine-1-carboxylate is relatively complicated and includes multiple steps. First, t-butanol is converted to a carboxylic acid ester compound by a chemical reaction. The carboxylic acid ester is then combined with the piperidine using an appropriate reagent and the methoxy and formyl functional groups are introduced by reaction. Finally, the carboxylic acid ester is converted to the desired compound by oxidation, protection and reaction.
Safety information: tert-Butyl 4-(2-methody-2-oxoacetyl)-3-oxopperidine-1-boxylate has no special safety risk information to report. However, as a chemical substance, it should comply with laboratory safety procedures and avoid direct contact with skin and eyes. If ingested or inhaled, seek medical help immediately.
Last Update：2024-04-09 21:01:54
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