(S)-叔丁基(哌啶-3-基甲基)氨基甲酸酯
(S)-3-N-Boc-Aminomethylpiperidine.HCL
CAS: 1016167-99-9
Molecular Formula: C11H23ClN2O2
(S)-叔丁基(哌啶-3-基甲基)氨基甲酸酯 - Names and Identifiers
| Name | (S)-3-N-Boc-Aminomethylpiperidine.HCL |
| Synonyms | S-3-N-BOC-AMINOMETHYL PIPERIDINE-HCl (S)-3-N-Boc-Aminomethylpiperidine.HCL tert-butyl [(3S)-3-piperidinylmethyl]carbamate hydrochloride (S)-tert-Butyl (piperidin-3-ylMethyl)carbaMate hydrochloride |
| CAS | 1016167-99-9 |
| InChI | InChI=1S/C11H22N2O2.ClH/c1-11(2,3)15-10(14)13-8-9-5-4-6-12-7-9;/h9,12H,4-8H2,1-3H3,(H,13,14);1H/t9-;/m0./s1 |
(S)-叔丁基(哌啶-3-基甲基)氨基甲酸酯 - Physico-chemical Properties
| Molecular Formula | C11H23ClN2O2 |
| Molar Mass | 250.76552 |
| Density | 0.981±0.06 g/cm3(Predicted) |
| Boling Point | 321.8±15.0 °C(Predicted) |
| pKa | 12.71±0.46(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
(S)-叔丁基(哌啶-3-基甲基)氨基甲酸酯 - Introduction
(S)-3-Boc-aminomethylpiperidine hydrochloride (also known as (S)-3-Boc-AMP hydrochloride) is an organic compound. The following is a description of its nature, use, formulation and safety information:
Nature:
-Appearance: White crystalline solid
-Molecular formula: C14H24N2O4 · HCl
-Molecular weight: 330.81g/mol
-Melting point: 165-170 degrees Celsius
-Solubility: Soluble in water and organic solvents, such as ethanol and dichloromethane.
Use:
- (S)-3-Boc-aminomethylpiperidine hydrochloride is a commonly used organic synthesis intermediate.
-It can be used as a precursor for the synthesis of β-lactam drugs and targeted tumor therapeutic drugs in drug synthesis.
- (S)-3-Boc-aminomethyl piperidine hydrochloride can also play an important role as a catalyst in enantioselective synthesis.
Preparation Method:
The preparation of- (S)-3-Boc-aminomethyl piperidine hydrochloride usually involves the following steps:
1. (S)-3-Boc-aminomethylpiperidine is reacted with hydrogen chloride to generate (S)-3-Boc-aminomethylpiperidine hydrochloride.
2. The pure product was extracted by crystallization, filtration and drying steps.
Safety Information:
- (S)-3-Boc-aminomethyl piperidine hydrochloride is generally a low-toxic compound, but it is still necessary to pay attention to safe operation.
-During use, wear appropriate protective gloves and glasses to avoid direct contact with skin and eyes.
-It should be operated in a well-ventilated place to avoid inhaling dust and steam.
-Should be stored in a dry, cool place, away from fire and flammable substances.
-If swallowed or exposed to the compound, seek medical help immediately and provide detailed compound information to your doctor.
Nature:
-Appearance: White crystalline solid
-Molecular formula: C14H24N2O4 · HCl
-Molecular weight: 330.81g/mol
-Melting point: 165-170 degrees Celsius
-Solubility: Soluble in water and organic solvents, such as ethanol and dichloromethane.
Use:
- (S)-3-Boc-aminomethylpiperidine hydrochloride is a commonly used organic synthesis intermediate.
-It can be used as a precursor for the synthesis of β-lactam drugs and targeted tumor therapeutic drugs in drug synthesis.
- (S)-3-Boc-aminomethyl piperidine hydrochloride can also play an important role as a catalyst in enantioselective synthesis.
Preparation Method:
The preparation of- (S)-3-Boc-aminomethyl piperidine hydrochloride usually involves the following steps:
1. (S)-3-Boc-aminomethylpiperidine is reacted with hydrogen chloride to generate (S)-3-Boc-aminomethylpiperidine hydrochloride.
2. The pure product was extracted by crystallization, filtration and drying steps.
Safety Information:
- (S)-3-Boc-aminomethyl piperidine hydrochloride is generally a low-toxic compound, but it is still necessary to pay attention to safe operation.
-During use, wear appropriate protective gloves and glasses to avoid direct contact with skin and eyes.
-It should be operated in a well-ventilated place to avoid inhaling dust and steam.
-Should be stored in a dry, cool place, away from fire and flammable substances.
-If swallowed or exposed to the compound, seek medical help immediately and provide detailed compound information to your doctor.
Last Update：2024-04-09 15:17:51
