Boc-NH-PEG2-Ms
t-Boc-N-Amido-PEG2-Ms
CAS: 302331-20-0
Molecular Formula: C10H21NO6S
Boc-NH-PEG2-Ms - Names and Identifiers
| Name | t-Boc-N-Amido-PEG2-Ms |
| Synonyms | Boc-N-PEG2-Ms Boc-N-PEG2-Oms Boc-NH-PEG2-Ms t-Boc-N-Amido-PEG2-Ms 2-(2-((tert-Butoxycarbonyl)amino)ethoxy)ethyl methanesulfonate |
| CAS | 302331-20-0 |
Boc-NH-PEG2-Ms - Physico-chemical Properties
| Molecular Formula | C10H21NO6S |
| Molar Mass | 283.34 |
Boc-NH-PEG2-Ms - Upstream Downstream Industry
| Downstream Products | Carbamic acid, [2-(2-aminoethoxy)ethyl]-, 1,1-dimethylethyl ester (9CI) |
Boc-NH-PEG2-Ms - Introduction
t-Boc-N-Amido-PEG2-Ms (t-Boc-N-Amido-PEG2-Ms) is a compound that has the following properties and uses:
Nature:
1. Appearance: white solid
2. Molecular formula: C25H48N2O10S
3. Molecular weight: 552.71g/mol
Use:
1. Biomedical research: t-Boc-N-Amido-PEG2-Ms can be used as modifiers for biomaterials and drugs to improve the solubility and stability of drugs, or to change the targeting and pharmacokinetics of drugs.
2. Catalyst: t-Boc-N-Amido-PEG2-Ms can be used as a catalyst for certain chemical reactions.
Method:
The method of preparing the t-Boc-N-Amido-PEG2-Ms is as follows:
1. The amino tert-butyl ester is reacted with dipolyethylene glycol in an appropriate solvent.
2. During the reaction, reagents such as thionyl chloride or nitrosobenzoyl chloride are added to generate Ester structures and protect amino groups.
3. Remove the protecting group (t-Boc) under appropriate conditions to obtain the target compound.
Safety Information:
1. t-Boc-N-Amido-PEG2-Ms is an organic compound that requires special laboratory operations and storage environments.
2. In the use of the process should follow the safety procedures, the use of appropriate personal protective equipment, such as gloves and glasses.
3. Avoid inhalation, ingestion or skin contact. In the case of accidental contact, rinse immediately with plenty of water and seek medical help.
4. Store away from fire and oxidant, keep the container sealed and avoid exposure to direct sunlight.
Please note that the above information is for reference only. Laboratory guidelines and safe operating procedures should be followed for specific operation and use.
Nature:
1. Appearance: white solid
2. Molecular formula: C25H48N2O10S
3. Molecular weight: 552.71g/mol
Use:
1. Biomedical research: t-Boc-N-Amido-PEG2-Ms can be used as modifiers for biomaterials and drugs to improve the solubility and stability of drugs, or to change the targeting and pharmacokinetics of drugs.
2. Catalyst: t-Boc-N-Amido-PEG2-Ms can be used as a catalyst for certain chemical reactions.
Method:
The method of preparing the t-Boc-N-Amido-PEG2-Ms is as follows:
1. The amino tert-butyl ester is reacted with dipolyethylene glycol in an appropriate solvent.
2. During the reaction, reagents such as thionyl chloride or nitrosobenzoyl chloride are added to generate Ester structures and protect amino groups.
3. Remove the protecting group (t-Boc) under appropriate conditions to obtain the target compound.
Safety Information:
1. t-Boc-N-Amido-PEG2-Ms is an organic compound that requires special laboratory operations and storage environments.
2. In the use of the process should follow the safety procedures, the use of appropriate personal protective equipment, such as gloves and glasses.
3. Avoid inhalation, ingestion or skin contact. In the case of accidental contact, rinse immediately with plenty of water and seek medical help.
4. Store away from fire and oxidant, keep the container sealed and avoid exposure to direct sunlight.
Please note that the above information is for reference only. Laboratory guidelines and safe operating procedures should be followed for specific operation and use.
Last Update：2024-04-09 15:18:02
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