boc-N-methyl-L-serine
boc-N-methyl-L-serine
CAS: 101772-29-6
Molecular Formula: C9H17NO5
boc-N-methyl-L-serine - Names and Identifiers
boc-N-methyl-L-serine - Physico-chemical Properties
| Molecular Formula | C9H17NO5 |
| Molar Mass | 219.24 |
| Density | 1?+-.0.06 g/cm3(Predicted) |
| Melting Point | 83-87°C |
| Boling Point | 353.2±42.0 °C(Predicted) |
| Appearance | Solid |
| BRN | 8685334 |
| pKa | 3.63±0.10(Predicted) |
| Storage Condition | Sealed in dry,Room Temperature |
boc-N-methyl-L-serine - Risk and Safety
| WGK Germany | 3 |
boc-N-methyl-L-serine - Introduction
Boc-N-Methyl-L-serine is an organic compound with the formula Boc-CH(NH2)COOH. In this structure, Boc represents t-butoxycarbonyl (tert-butoxycarbonyl),N-methyl indicates that the amino group has a methyl group, and L-serine indicates that the amino group has a serine group.
Boc-N-methyl-L-serine is an amino acid protecting group commonly used in peptide synthesis and chemical modification. Its main uses include:
1. As a starting material for synthetic peptides, the reactivity of the amino terminal can be protected for subsequent chemical modification or synthesis.
2. as an amino acid protecting group to prevent other reactants or reagents for non-selective reaction of amino acids.
The production method of Boc-N-methyl-L-serine is generally obtained by reacting L-serine with tert-butoxycarbonyl chloroformate (t-boc chloride) under highly alkaline conditions for methylation. The specific preparation method can be consulted through the literature or chemical synthesis manual.
Regarding safety information, Boc-N-methyl-L-serine is an organic compound. The following matters should be paid attention to during operation:
1. Need to operate in a well-ventilated laboratory environment to avoid inhalation of dust or volatiles.
2. Pay attention to avoid contact with skin, eyes or mucous membranes. If contact occurs, please rinse with plenty of water immediately and seek medical attention in time.
3. Follow proper experimental procedures and safety practices, including wearing personal protective equipment (e. g., lab gloves, goggles, etc.).
4. store the compound in a dry, dark place, away from fire and oxidant, avoid mixing with other chemicals.
Boc-N-methyl-L-serine is an amino acid protecting group commonly used in peptide synthesis and chemical modification. Its main uses include:
1. As a starting material for synthetic peptides, the reactivity of the amino terminal can be protected for subsequent chemical modification or synthesis.
2. as an amino acid protecting group to prevent other reactants or reagents for non-selective reaction of amino acids.
The production method of Boc-N-methyl-L-serine is generally obtained by reacting L-serine with tert-butoxycarbonyl chloroformate (t-boc chloride) under highly alkaline conditions for methylation. The specific preparation method can be consulted through the literature or chemical synthesis manual.
Regarding safety information, Boc-N-methyl-L-serine is an organic compound. The following matters should be paid attention to during operation:
1. Need to operate in a well-ventilated laboratory environment to avoid inhalation of dust or volatiles.
2. Pay attention to avoid contact with skin, eyes or mucous membranes. If contact occurs, please rinse with plenty of water immediately and seek medical attention in time.
3. Follow proper experimental procedures and safety practices, including wearing personal protective equipment (e. g., lab gloves, goggles, etc.).
4. store the compound in a dry, dark place, away from fire and oxidant, avoid mixing with other chemicals.
Last Update：2024-04-09 19:05:44
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