N-(tert-butoxycarbonyl)alanylproline
Boc-Ala-Pro-OH
CAS: 33300-72-0
Molecular Formula: C13H22N2O5
N-(tert-butoxycarbonyl)alanylproline - Names and Identifiers
| Name | Boc-Ala-Pro-OH |
| Synonyms | Boc-AP Boc-Ala-Pro BOC-ALA-PRO-OH Boc-Ala-Pro-OH Boc-L-Ala-L-Pro Boc-L-Ala-L-Pro-OH N-(tert-butoxycarbonyl)alanylproline 1-[N-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl]-L-proline (S)-1-((S)-2-((tert-Butoxycarbonyl)amino)propanoyl)pyrrolidine-2-carboxylic acid |
| CAS | 33300-72-0 |
| InChI | InChI=1/C13H22N2O5/c1-8(14-12(19)20-13(2,3)4)10(16)15-7-5-6-9(15)11(17)18/h8-9H,5-7H2,1-4H3,(H,14,19)(H,17,18) |
N-(tert-butoxycarbonyl)alanylproline - Physico-chemical Properties
| Molecular Formula | C13H22N2O5 |
| Molar Mass | 286.32 |
| Density | 1.218g/cm3 |
| Boling Point | 491.451°C at 760 mmHg |
| Flash Point | 251.021°C |
| Vapor Presure | 0mmHg at 25°C |
| Storage Condition | Sealed in dry,2-8°C |
| Refractive Index | 1.511 |
N-(tert-butoxycarbonyl)alanylproline - Risk and Safety
| WGK Germany | 3 |
N-(tert-butoxycarbonyl)alanylproline - Introduction
Boc-Ala-Pro-OH(Boc-Ala-Pro-OH) is an organic compound whose chemical structure is a combination of N-tert-butoxycarbonyl protecting group and acetamidoisovaleric acid (Ala-Pro).
Nature:
Boc-Ala-Pro-OH is a white crystalline solid that is stable at room temperature. Its molecular formula is C15H25NO5 and its relative molecular mass is 303.36. It has high solubility in solvents such as chloroform, dimethylformamide and dichloromethane, and is insoluble in water.
Use:
Boc-Ala-Pro-OH are commonly used as amino acid protecting groups in organic synthesis to protect amino acid or polypeptide sequences. It can be synthesized by reacting a substrate of an amino acid with BOC-acetic anhydride.
Method:
The preparation of Boc-Ala-Pro-OH is mainly accomplished by reacting acetic anhydride with a protected amino group. The specific synthesis process can refer to the professional organic synthesis literature.
Safety Information:
The Boc-Ala-Pro-OH is relatively safe under normal operating conditions. However, care should be taken to avoid inhalation of dust or contact with the skin and eyes. Wear protective gloves and goggles and operate in a well-ventilated environment. If careless contact, should be promptly washed with plenty of water. At the same time, the use and storage, to follow the corresponding safety procedures and storage conditions.
Nature:
Boc-Ala-Pro-OH is a white crystalline solid that is stable at room temperature. Its molecular formula is C15H25NO5 and its relative molecular mass is 303.36. It has high solubility in solvents such as chloroform, dimethylformamide and dichloromethane, and is insoluble in water.
Use:
Boc-Ala-Pro-OH are commonly used as amino acid protecting groups in organic synthesis to protect amino acid or polypeptide sequences. It can be synthesized by reacting a substrate of an amino acid with BOC-acetic anhydride.
Method:
The preparation of Boc-Ala-Pro-OH is mainly accomplished by reacting acetic anhydride with a protected amino group. The specific synthesis process can refer to the professional organic synthesis literature.
Safety Information:
The Boc-Ala-Pro-OH is relatively safe under normal operating conditions. However, care should be taken to avoid inhalation of dust or contact with the skin and eyes. Wear protective gloves and goggles and operate in a well-ventilated environment. If careless contact, should be promptly washed with plenty of water. At the same time, the use and storage, to follow the corresponding safety procedures and storage conditions.
Last Update：2024-04-10 22:29:15
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CAS: 33300-72-0
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Mobile: 18021002903
QQ: 3008007409
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