Boc-D-2-(3-Thienyl)-glycine
Boc-D-2-(3-Thienyl)-glycine
CAS:
Molecular Formula: C11H15NO4S
Boc-D-2-(3-Thienyl)-glycine - Names and Identifiers
| Name | Boc-D-2-(3-Thienyl)-glycine |
| Synonyms | Boc-D-2-(3-Thienyl)-glycine |
Boc-D-2-(3-Thienyl)-glycine - Physico-chemical Properties
| Molecular Formula | C11H15NO4S |
| Molar Mass | 257.3061 |
Boc-D-2-(3-Thienyl)-glycine - Introduction
Boc-D-2-(3-Thienyl)-glycine is an organic compound which is linked to D-2-(3-thienyl) glycine by a protecting group (Boc). Its molecular formula is C14H19NO4S and its relative molecular mass is 297.38g/mol.
The properties of Boc-D-2-(3-Thienyl)-glycine mainly include: colorless solid, with special smell. It has moderate solubility and is soluble in common solvents such as methanol, dimethyl sulfoxide and dichloromethane. It is stable at room temperature.
Boc-D-2-(3-Thienyl)-glycine is mainly used in peptide synthesis and drug research in organic synthesis. As a protective amino acid, it can be synthesized by reacting with other amino acids. In pharmaceutical research, it can also be used as a synthetic intermediate for drugs.
The preparation of Boc-D-2-(3-Thienyl)-glycine is generally obtained by chemical synthesis. The specific synthetic route depends on the specific reaction conditions and reactants, and generally involves the introduction of the thiophene group, the acylation reaction, and finally the Boc protection. The synthesis process requires certain chemical knowledge and technology.
Regarding safety information, Boc-D-2-(3-Thienyl)-glycine generally have low toxicity under normal conditions of use. However, for use in chemical laboratories, general laboratory safety regulations need to be observed, such as wearing appropriate protective equipment (such as gloves and laboratory glasses), avoiding exposure to skin and eyes, and good ventilation. At the same time, during storage and handling, care should be taken to avoid contact with strong oxidants and strong acids to avoid dangerous reactions. If skin contact or inhalation problems occur, seek medical attention immediately.
The properties of Boc-D-2-(3-Thienyl)-glycine mainly include: colorless solid, with special smell. It has moderate solubility and is soluble in common solvents such as methanol, dimethyl sulfoxide and dichloromethane. It is stable at room temperature.
Boc-D-2-(3-Thienyl)-glycine is mainly used in peptide synthesis and drug research in organic synthesis. As a protective amino acid, it can be synthesized by reacting with other amino acids. In pharmaceutical research, it can also be used as a synthetic intermediate for drugs.
The preparation of Boc-D-2-(3-Thienyl)-glycine is generally obtained by chemical synthesis. The specific synthetic route depends on the specific reaction conditions and reactants, and generally involves the introduction of the thiophene group, the acylation reaction, and finally the Boc protection. The synthesis process requires certain chemical knowledge and technology.
Regarding safety information, Boc-D-2-(3-Thienyl)-glycine generally have low toxicity under normal conditions of use. However, for use in chemical laboratories, general laboratory safety regulations need to be observed, such as wearing appropriate protective equipment (such as gloves and laboratory glasses), avoiding exposure to skin and eyes, and good ventilation. At the same time, during storage and handling, care should be taken to avoid contact with strong oxidants and strong acids to avoid dangerous reactions. If skin contact or inhalation problems occur, seek medical attention immediately.
Last Update：2024-04-09 21:11:58
