tert-butyl N-[(2R)-1-(benzylamino)-3-hydroxy-1-oxopropan-2-yl]carbamate - Names and Identifiers
tert-butyl N-[(2R)-1-(benzylamino)-3-hydroxy-1-oxopropan-2-yl]carbamate - Physico-chemical Properties
Molecular Formula | C15H22N2O4
|
Molar Mass | 294.35 |
Density | 1.159±0.06 g/cm3(Predicted) |
Boling Point | 532.9±50.0 °C(Predicted) |
pKa | 10.62±0.46(Predicted) |
Storage Condition | 2-8°C |
tert-butyl N-[(2R)-1-(benzylamino)-3-hydroxy-1-oxopropan-2-yl]carbamate - Introduction
Boc-D-Serine BenzylaMide, also known as Boc-D-Serine Benzylamide, is an organic compound.
The compound is a white or almost white solid with good solubility. Its molecular formula is C19H27N3O4 and its relative molecular mass is 369.44g/mol.
The main use of Boc-D-Serine Benzylamide is as a reagent and intermediate in organic synthesis. It is commonly used in the synthesis of polypeptides and pharmaceutical compounds. Its derivatives are also used as research reagents in pharmaceutical research and biomedical fields.
The basic steps for the preparation of Boc-D-Serine Benzylamide are as follows:
1. Benzylamine is reacted with tert-butyl bromoformate to obtain tert-butyl benzylamine formate.
2. Reaction of tert-butyl benzylformate with (L)-serine (D-serine) to give Benzylamide Boc-D-Serine.
Because Boc-D-Serine Benzylamide is an organic compound, you need to pay attention to safety when using it. It may be irritating to the eyes, skin and respiratory tract, so wear appropriate protective measures during operation. At the same time, avoid contact with oxidants and strong acids to prevent reaction.
Last Update:2024-04-09 21:11:58