N-Boc-N-methyl-L-tryptophan
Boc-Nalpha-methyl-L-tryptophan
CAS: 141408-33-5
Molecular Formula: C17H22N2O4
N-Boc-N-methyl-L-tryptophan - Names and Identifiers
N-Boc-N-methyl-L-tryptophan - Physico-chemical Properties
| Molecular Formula | C17H22N2O4 |
| Molar Mass | 318.37 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD02682368 |
N-Boc-N-methyl-L-tryptophan - Risk and Safety
| Hazard Class | IRRITANT |
N-Boc-N-methyl-L-tryptophan - Introduction
Boc-Nalpha-methyl-L-tryptophan(Boc-Nalpha-methyl-L-tryptophan) is an organic compound. Its chemical formula is C17H22N2O4, and its structure contains carboxylic acid groups, methyl groups, tryptophan residues and propanol groups.
Boc-Nalpha-methyl-L-tryptophan are mainly used as reagents and synthetic intermediates in research. It is often used in the synthesis of peptides and proteins, with the role of regulating protein structure and function. In addition, it can be used as a chemical tool in drug research and development.
The preparation Boc-Nalpha-methyl-L-tryptophan usually adopts organic synthesis method. One common method is to react L-tryptophan with methylmagnesium bromide to give methylated L-tryptophan, which is then reacted with Boc-OH to give Boc-L-tryptophan. Finally, by reaction with 1,1-dimethylethoxy/propanol, the target product is obtained.
Regarding safety information, Boc-Nalpha-methyl-L-tryptophan it is relatively safe under general conditions, it is still necessary to pay attention to correct experimental operation and use. It is a chemical that can cause irritation and damage to the human body. When using and handling the compound, it is necessary to use personal protective equipment, such as laboratory gloves, goggles and protective clothing, and to operate in a well-ventilated area. If exposed to the compound by accident, rinse immediately with plenty of water and seek medical help.
Boc-Nalpha-methyl-L-tryptophan are mainly used as reagents and synthetic intermediates in research. It is often used in the synthesis of peptides and proteins, with the role of regulating protein structure and function. In addition, it can be used as a chemical tool in drug research and development.
The preparation Boc-Nalpha-methyl-L-tryptophan usually adopts organic synthesis method. One common method is to react L-tryptophan with methylmagnesium bromide to give methylated L-tryptophan, which is then reacted with Boc-OH to give Boc-L-tryptophan. Finally, by reaction with 1,1-dimethylethoxy/propanol, the target product is obtained.
Regarding safety information, Boc-Nalpha-methyl-L-tryptophan it is relatively safe under general conditions, it is still necessary to pay attention to correct experimental operation and use. It is a chemical that can cause irritation and damage to the human body. When using and handling the compound, it is necessary to use personal protective equipment, such as laboratory gloves, goggles and protective clothing, and to operate in a well-ventilated area. If exposed to the compound by accident, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 21:00:56
