9H-fluoren-9-ylmethyl (4S)-4-methyl-2,5-dioxo-1,3-oxazolidine-3-carboxylate
fmoc-L-alanine N-carboxy anhydride
CAS: 125814-20-2
Molecular Formula: C19H15NO5
9H-fluoren-9-ylmethyl (4S)-4-methyl-2,5-dioxo-1,3-oxazolidine-3-carboxylate - Names and Identifiers
9H-fluoren-9-ylmethyl (4S)-4-methyl-2,5-dioxo-1,3-oxazolidine-3-carboxylate - Physico-chemical Properties
| Molecular Formula | C19H15NO5 |
| Molar Mass | 337.33 |
9H-fluoren-9-ylmethyl (4S)-4-methyl-2,5-dioxo-1,3-oxazolidine-3-carboxylate - Introduction
FMOC-L-alanine-N-carboxyl-endocyclic anhydride is an organic compound whose chemical formula is C27H22N2O6 and whose chemical name is N-hydroxysuccinimide ester. The following is an introduction to its nature, use, preparation and safety information:
Nature:
-Appearance: Common white or yellowish solid
-melting point: about 175-177 ℃
-Solubility: It has a certain solubility in some organic solvents (such as dimethylformamide, dichloromethane).
Use:
FMOC-L-alanine-N-carboxy-endocyclic anhydride is commonly used in peptide synthesis reactions in solid phase synthesis and chemical synthesis. It is a peptide synthesis of the protecting group, can protect the amino acid. In the synthesis of polypeptides, specific amino acids can be added by FMOC-L-alanine-N-carboxy-endocyclic anhydride. In addition, it can also be used as an active reagent in other organic synthesis reactions.
Method:
FMOC-L-alanine-N-carboxy-endocyclic anhydride is generally prepared by reacting FMOC-L-alanine and N-carboxy-endocyclic anhydride. The common preparation method in chemical synthesis is to carry out the reaction under alkaline conditions, and the desired product is obtained by adding an organic solvent and suitable reaction time.
Safety Information:
- FMOC-L-alanine-N-carboxy-cyclic anhydride is a potentially hazardous chemical and should be handled in an appropriate laboratory environment.
-Follow safe practices when using, including wearing appropriate personal protective equipment (e. g. lab gloves, glasses and lab coats).
-Avoid direct contact with skin and eyes. During operation, care needs to be taken to avoid inhalation or ingestion of the compound.
-If taken by mistake or if any discomfort occurs, consult a doctor immediately and bring the relevant label or safety data sheet to consult a doctor.
Nature:
-Appearance: Common white or yellowish solid
-melting point: about 175-177 ℃
-Solubility: It has a certain solubility in some organic solvents (such as dimethylformamide, dichloromethane).
Use:
FMOC-L-alanine-N-carboxy-endocyclic anhydride is commonly used in peptide synthesis reactions in solid phase synthesis and chemical synthesis. It is a peptide synthesis of the protecting group, can protect the amino acid. In the synthesis of polypeptides, specific amino acids can be added by FMOC-L-alanine-N-carboxy-endocyclic anhydride. In addition, it can also be used as an active reagent in other organic synthesis reactions.
Method:
FMOC-L-alanine-N-carboxy-endocyclic anhydride is generally prepared by reacting FMOC-L-alanine and N-carboxy-endocyclic anhydride. The common preparation method in chemical synthesis is to carry out the reaction under alkaline conditions, and the desired product is obtained by adding an organic solvent and suitable reaction time.
Safety Information:
- FMOC-L-alanine-N-carboxy-cyclic anhydride is a potentially hazardous chemical and should be handled in an appropriate laboratory environment.
-Follow safe practices when using, including wearing appropriate personal protective equipment (e. g. lab gloves, glasses and lab coats).
-Avoid direct contact with skin and eyes. During operation, care needs to be taken to avoid inhalation or ingestion of the compound.
-If taken by mistake or if any discomfort occurs, consult a doctor immediately and bring the relevant label or safety data sheet to consult a doctor.
Last Update：2024-04-10 22:29:15
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