4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) - Names and Identifiers
Name | 4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI)
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Synonyms | N-Boc-(4-Pyridyl)-DL-Alanine Boc-DL-3-(4-Pyridyl)-alanine Boc-3-(4-Pyridyl)-DL-alanine 2-{[(tert-Butoxy)carbonyl]amino}-3-(pyridin-4-yl)-propanoic acid 4-Pyridinepropionicacid, a-(carboxyamino)-, N-tert-butylester (8CI) 4-Pyridinepropionic acid, α-(carboxyamino)-, N-tert-butyl ester (8CI) 4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) 4-Pyridinepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]- (9CI)
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CAS | 33814-94-7
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4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) - Physico-chemical Properties
Molecular Formula | C13H18N2O4
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Molar Mass | 266.29 |
Storage Condition | 2-8°C |
4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) - Risk and Safety
4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) - Introduction
4-Pyridinepropanoicacid, a-[[(1,1-dimenthylethoxy) carbonyl]amino]-(9CI), also known as 4-pyridylpropionic acid, is an organic compound with the chemical formula C12H17NO4.
Nature:
4-Pyridinepropanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) is a colorless or slightly yellow solid with a pyridine fragrance. It is a compound having weak acidity and can be dissolved in organic solvents such as ethanol, dimethylformamide and dichloromethane.
Use:
4-Pyridinepropanoic acid, a-[[(1,1-dimenthylethoxy) carbonyl]amino]-(9CI) is an important organic reagent, which is widely used in synthetic chemistry. It is often used as a protecting group for amino acids. By protecting the carboxyl group of amino acids, selective chemical reactions can be carried out to control the progress and selectivity of the reaction. In addition, the compound can also be used in the field of peptide synthesis and drug research.
Preparation Method:
4-Pyridinepropanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) is generally synthesized by organic synthetic chemical methods. Specific steps include reacting 4-pyridylpropionic acid with N,N'-dimethylcarbodiimide (DMC) to form an intermediate product, then protecting the intermediate product as a Boc amido group using chloroformyl chloride (ClCOCl), and finally protecting the hydroxyl group with an ether ester. This gives 4-Pyridinepropanoic acid, a-[[(1,1-dimenthylethoxy) carbonyl]amino]-(9CI).
Safety Information:
4-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) is a chemical substance, which should be paid attention to during use and storage. It may be irritating to the skin, eyes and respiratory system and direct contact must be avoided. Wear appropriate protective gloves and glasses and maintain a well-ventilated laboratory environment. If you come into contact with this compound, rinse immediately with plenty of water and seek medical help. In addition, avoid contact with oxidants and high temperature conditions during storage.
Last Update:2024-04-09 20:52:54