(±)-2-Amino-1-propanol-1,1,2,3,3-d6-N-t-BOC

(±)-2-Amino-1-propanol-1,1,2,3,3-d6-N-t-BOC, also known as N-tert-butoxycarbonyl-2-amino-1-propanol-d6, is a deuterated derivative of N-tert-butoxycarbonyl-2-amino-1-propanol. It is primarily used as a reagent in organic synthesis for the preparation of peptides and as a building block in the synthesis of other organic compounds. The chemical structure of (±)-2-Amino-1-propanol-1,1,2,3,3-d6-N-t-BOC consists of a primary amino group and a hydroxyl group on a propane backbone, with a tert-butoxycarbonyl (BOC) protecting group attached to the amino group. The deuterium atoms are incorporated to allow for easier analysis using mass spectrometry. The BOC group is used to protect the amino group during synthetic reactions and can be removed under acidic conditions to expose the amino group for further reaction. In addition to its use in organic synthesis, (±)-2-Amino-1-propanol-1,1,2,3,3-d6-N-t-BOC has also been studied for its potential therapeutic applications. It has been shown to have antioxidant and anti-inflammatory properties, and there is ongoing research into its potential as a treatment for conditions such as Alzheimer's disease and Parkinson's disease. Overall, (±)-2-Amino-1-propanol-1,1,2,3,3-d6-N-t-BOC is a versatile reagent with a range of applications in organic synthesis, as well as potential therapeutic uses. Its incorporation of deuterium atoms allows for easier analysis, making it a valuable tool for researchers in a variety of fields.