(2S)-5-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name)
N-tert-Butoxycarbonyl-L-glutamic acid gamma-tert-butyl ester
CAS: 13726-84-6
Molecular Formula: C14H25NO6
(2S)-5-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) - Names and Identifiers
(2S)-5-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) - Physico-chemical Properties
| Molecular Formula | C14H25NO6 |
| Molar Mass | 303.35 |
| Density | 1.121±0.06 g/cm3(Predicted) |
| Melting Point | 102-105°C |
| Boling Point | 449.8±40.0 °C(Predicted) |
| Flash Point | 225.8°C |
| Vapor Presure | 2.42E-09mmHg at 25°C |
| Appearance | White powder |
| BRN | 2149791 |
| pKa | 3.82±0.10(Predicted) |
| Storage Condition | 2-8°C |
| Refractive Index | 1.47 |
| MDL | MFCD00038257 |
(2S)-5-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) - Risk and Safety
| WGK Germany | 3 |
| HS Code | 2924 19 00 |
(2S)-5-tert-butoxy-2-[(tert-butoxycarbonyl)amino]-5-oxopentanoic acid (non-preferred name) - Introduction
tert-Butoxycarbonyl-L-glutamic acid 5 tert-butyl ester, also known as BOC-L-glutamic acid 5-tert-butyl ester, is an organic compound. Its chemical properties are as follows:
1. Appearance: Colorless crystalline solid.
2. molecular formula: C15H25NO6.
3. Relative molecular mass: 315.36.
4. solubility: soluble in organic solvents such as methanol, ethanol and dichloromethane, insoluble in water.
tert-butyloxycarbonyl-L-glutamic acid 5 tert-butyl ester is mainly used as follows:
1. organic synthesis: can be used as a protective group in peptide synthesis.
2. biochemical research: can be used as a reagent to study cell signaling and metabolism.
The method for preparing tert-butoxycarbonyl-L-glutamic acid 5 tert-butyl ester is as follows:
L-glutamic acid is reacted with t-butyl carbonate under alkaline conditions to produce the target product. Typically, the reaction is carried out in an anhydrous organic solvent, such as dimethylformamide (DMF) or dichloromethane.
Regarding safety information, it is generally believed that tert-butoxycarbonyl-L-glutamic acid 5 tert-butyl ester is relatively stable and non-toxic. However, it is still recommended to wear appropriate personal protective equipment during use and avoid direct contact with skin, eyes and respiratory tract. If taken by mistake or inhaled by mistake, please seek medical attention in time.
Please note that the above information is for reference only. Laboratory operating specifications and safety guidelines should be followed in specific use, and risks should be evaluated and controlled according to specific conditions.
1. Appearance: Colorless crystalline solid.
2. molecular formula: C15H25NO6.
3. Relative molecular mass: 315.36.
4. solubility: soluble in organic solvents such as methanol, ethanol and dichloromethane, insoluble in water.
tert-butyloxycarbonyl-L-glutamic acid 5 tert-butyl ester is mainly used as follows:
1. organic synthesis: can be used as a protective group in peptide synthesis.
2. biochemical research: can be used as a reagent to study cell signaling and metabolism.
The method for preparing tert-butoxycarbonyl-L-glutamic acid 5 tert-butyl ester is as follows:
L-glutamic acid is reacted with t-butyl carbonate under alkaline conditions to produce the target product. Typically, the reaction is carried out in an anhydrous organic solvent, such as dimethylformamide (DMF) or dichloromethane.
Regarding safety information, it is generally believed that tert-butoxycarbonyl-L-glutamic acid 5 tert-butyl ester is relatively stable and non-toxic. However, it is still recommended to wear appropriate personal protective equipment during use and avoid direct contact with skin, eyes and respiratory tract. If taken by mistake or inhaled by mistake, please seek medical attention in time.
Please note that the above information is for reference only. Laboratory operating specifications and safety guidelines should be followed in specific use, and risks should be evaluated and controlled according to specific conditions.
Last Update：2024-04-10 22:29:15
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