Boc-(R)-3-Amino-5-hexynoic acid
Boc-(R)-3-Amino-5-hexynoic acid
CAS:
Molecular Formula: C11H17NO4
Boc-(R)-3-Amino-5-hexynoic acid - Names and Identifiers
Boc-(R)-3-Amino-5-hexynoic acid - Physico-chemical Properties
| Molecular Formula | C11H17NO4 |
| Molar Mass | 227.257 |
| Storage Condition | 2-8℃ |
Boc-(R)-3-Amino-5-hexynoic acid - Introduction
Boc-(R)-3-Amino-5-hexynoic acid is an organic compound with the following properties:
1. Appearance and physical properties: Boc-(R)-3-Amino-5-hexynoic acid is a white crystalline solid, soluble in organic solvents such as dichloromethane and ethanol.
2. structure and chemical properties: the compound contains 3-amino -5-alkynyl hexanoic acid structure, and has a protecting group Boc(t-butoxycarbonyl). Its levorotatory or dextrorotatory isomer (R or S) is due to its chiral center.
The main uses of Boc-(R)-3-Amino-5-hexynoic acid include:
1. Organic synthesis: It is a commonly used amino acid protecting group, which can be used as a starting material for drug synthesis and protein/peptide synthesis.
The method of preparing Boc-(R)-3-Amino-5-hexynoic acid usually involves the following steps:
1. take 3-amino -5-alkynyl hexanoic acid as raw material.
2. The amino acid is linked to the Boc protecting group by chemical reaction.
3. The product with higher purity is prepared by crystallization and purification steps.
For the safety information of Boc-(R)-3-Amino-5-hexynoic acid, the following are some considerations:
1. Avoid contact with skin and eyes. If there is contact, rinse immediately with plenty of water.
2. Good laboratory practices and safety measures should be taken during use and handling, including wearing protective gloves, glasses and laboratory coats.
3. Avoid using in places where there is no wind to prevent the concentration of harmful substances from increasing.
4. storage should be away from heat, fire and oxidant.
1. Appearance and physical properties: Boc-(R)-3-Amino-5-hexynoic acid is a white crystalline solid, soluble in organic solvents such as dichloromethane and ethanol.
2. structure and chemical properties: the compound contains 3-amino -5-alkynyl hexanoic acid structure, and has a protecting group Boc(t-butoxycarbonyl). Its levorotatory or dextrorotatory isomer (R or S) is due to its chiral center.
The main uses of Boc-(R)-3-Amino-5-hexynoic acid include:
1. Organic synthesis: It is a commonly used amino acid protecting group, which can be used as a starting material for drug synthesis and protein/peptide synthesis.
The method of preparing Boc-(R)-3-Amino-5-hexynoic acid usually involves the following steps:
1. take 3-amino -5-alkynyl hexanoic acid as raw material.
2. The amino acid is linked to the Boc protecting group by chemical reaction.
3. The product with higher purity is prepared by crystallization and purification steps.
For the safety information of Boc-(R)-3-Amino-5-hexynoic acid, the following are some considerations:
1. Avoid contact with skin and eyes. If there is contact, rinse immediately with plenty of water.
2. Good laboratory practices and safety measures should be taken during use and handling, including wearing protective gloves, glasses and laboratory coats.
3. Avoid using in places where there is no wind to prevent the concentration of harmful substances from increasing.
4. storage should be away from heat, fire and oxidant.
Last Update：2024-04-09 21:04:16
