BOC-3-(3-PYRIDYL)-DL-ALANINE

BOC-3-(3-PYRIDYL)-DL-ALANINE - Names and Identifiers

Name	2-TERT-BUTOXYCARBONYLAMINO-3-PYRIDIN-3-YL-PROPIONIC ACID
Synonyms	RARECHEM AK ML 0055 BOC-3-(3-PYRIDYL)-DL-ALANINE 2-TERT-BUTOXYCARBONYLAMINO-3-PYRIDIN-3-YL-PROPIONIC ACID 2-(tert-butoxycarbonylaMino)-3-(pyridin-3-yl)propanoic acid 3-Pyridinepropanoicacid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-(9CI) 3-Pyridinepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (±)- 3-Pyridinepropanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]- (9CI)
CAS	105454-25-9

BOC-3-(3-PYRIDYL)-DL-ALANINE - Physico-chemical Properties

Molecular Formula	C13H18N2O4
Molar Mass	266.29
Density	1.200±0.06 g/cm3(Predicted)
Boling Point	452.9±40.0 °C(Predicted)
pKa	3.43±0.10(Predicted)
Storage Condition	2-8°C

BOC-3-(3-PYRIDYL)-DL-ALANINE - Introduction

Boc-3-(3-pyridyl)-DL-alanine is an organic compound. Its molecular formula is C13H20N2O4 and its molecular weight is 268.31g/mol. It is characterized by having a Boc(tert-butylaminocarbonyl) protecting group and a 3-(3-pyridyl)-DL-alanine group.

Boc-3-(3-pyridyl)-DL-alanine can be used for amino protection reaction and deprotection reaction in organic synthesis. The Boc group can protect the active amino group under specific conditions to avoid reaction with other chemical reagents. This makes it of great significance in synthetic peptides and drug research.

A method for preparing Boc-3-(3-pyridyl)-DL-alanine is generally obtained by reacting 3-(3-pyridyl)-DL-alanine with tert-butylaminochloroformate (BOC-Cl). The reaction is usually carried out under basic conditions, and the formation of Boc-3-(3-pyridyl)-DL-alanine is accompanied by the formation of hydrogen chloride.

Regarding safety information, Boc-3-(3-pyridyl)-DL-alanine is a reagent generally used in organic chemistry laboratories. When using this compound, strictly follow laboratory practices and wear appropriate personal protective equipment, such as laboratory gloves and goggles. In addition, the compound should be handled with care to avoid direct contact with the skin and inhalation of its vapors. If the compound is accidentally exposed or inhaled, rinse immediately with water and seek medical help.

Last Update：2024-04-09 20:52:54