1076197-03-9

Basic information

• Product Name: (R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid
• Synonyms: a-[(Boc-amino)methyl]-1-naphthalenepropanoic acid;(R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid;3-((tert-Butoxycarbonyl)amino)-2-(naphthalen-1-ylmethyl)propanoic acid
• CAS NO: 1076197-03-9
• Molecular Formula: C19H23NO4
• Molecular Weight: 329.39022
• Mol File: 1076197-03-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid(1076197-03-9)
• EPA Substance Registry System: (R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid(1076197-03-9)

Safety Data

• Hazardous Substances Data: 1076197-03-9(Hazardous Substances Data)

Usage

General Description

(R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid, also known as (R,S)-Boc-napABOP, is a chiral compound containing a Boc-protected amino group and a naphthalen-1-ylmethyl moiety. It is commonly used as a building block in organic synthesis for the preparation of various pharmaceuticals and biological molecules. (R,S)-Boc-3-amino-2-(naphthalen-1-ylmethyl)-propionic acid is capable of forming stable amide bonds and can serve as a potential tool for the efficient synthesis of diverse chemical entities. The presence of a chiral center in the molecule gives it stereochemical properties, making it a valuable building block for the synthesis of compounds with specific stereochemistry. Additionally, the naphthalen-1-ylmethyl group contributes to the overall molecular structure and may impart unique chemical and biological properties to the resulting compounds.