3-Amino-1-Boc-3-methyl-az...
1-Boc-3-amino-3-methyl-azetidine
CAS: 1158758-77-0
Molecular Formula: C9H18N2O2
3-Amino-1-Boc-3-methyl-az... - Names and Identifiers
3-Amino-1-Boc-3-methyl-az... - Physico-chemical Properties
| Molecular Formula | C9H18N2O2 |
| Molar Mass | 186.25 |
| Density | 1.062±0.06 g/cm3(Predicted) |
| Boling Point | 242.5±33.0 °C(Predicted) |
| pKa | 8.29±0.20(Predicted) |
| Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
| Sensitive | Irritant |
| MDL | MFCD12408556 |
3-Amino-1-Boc-3-methyl-az... - Introduction
1-Boc-3-amino -3-methyl azetidine, chemical name is 3-((tert-butoxycarbonyl)amino)-3-methylbutyline, usually referred to as Boc-Arg.
Properties: 1-Boc-3-amino-3-methylazetidine is a white or off-white solid, soluble in organic solvents such as dimethylformamide (DMF) or dichloromethane.
Uses: 1-Boc-3-amino-3-methylazidine is a commonly used protected amine group, which is often used to protect amino groups in organic synthesis. It can be removed by a deprotection reaction to give the free amino group. Boc-Arg are also commonly used in the fields of peptide synthesis and pharmaceutical research.
preparation method: 1-Boc-3-amino -3-methyl azetidine preparation method is more diverse, the usual method is to form 3-amino -3-methyl azetidine, and then react with tert-butoxycarbonyl chloride methylene to obtain 1-Boc-3-amino -3-methyl azetidine.
Safety information: 1-Boc-3-amino-3-methyazetidine has low toxicity, but it still needs to pay attention to its possible irritation and sensitivity. Appropriate protective measures, such as lab gloves and goggles, should be worn during use.
Properties: 1-Boc-3-amino-3-methylazetidine is a white or off-white solid, soluble in organic solvents such as dimethylformamide (DMF) or dichloromethane.
Uses: 1-Boc-3-amino-3-methylazidine is a commonly used protected amine group, which is often used to protect amino groups in organic synthesis. It can be removed by a deprotection reaction to give the free amino group. Boc-Arg are also commonly used in the fields of peptide synthesis and pharmaceutical research.
preparation method: 1-Boc-3-amino -3-methyl azetidine preparation method is more diverse, the usual method is to form 3-amino -3-methyl azetidine, and then react with tert-butoxycarbonyl chloride methylene to obtain 1-Boc-3-amino -3-methyl azetidine.
Safety information: 1-Boc-3-amino-3-methyazetidine has low toxicity, but it still needs to pay attention to its possible irritation and sensitivity. Appropriate protective measures, such as lab gloves and goggles, should be worn during use.
Last Update：2024-04-09 02:00:41
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View History
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