1187667-02-2

Basic information

• Product Name: FMOC-2-AMINO-2-METHYLPROPANOL
• Synonyms: FMOC-AIB-OL;FMOC-2-AMINO-2-METHYLPROPANOL;FMOC-BETA-AMINOISOBUTANOL;N-(9-FLUORENYLMETHOXYCARBONYL)-BETA-AMINO-ISOBUTYL ALCOHOL;9H-Fluoren-9-ylmethyl 2-hydroxy-1,1-dimethylethylcarbamate
• CAS NO: 1187667-02-2
• Molecular Formula: C₁₉H₂₁NO₃
• Molecular Weight: 311.37
• Mol File: 1187667-02-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 506.4±33.0 °C(Predicted)
• Appearance: /
• Density: 1.189±0.06 g/cm3(Predicted)
• PKA: 11.61±0.46(Predicted)
• CAS DataBase Reference: FMOC-2-AMINO-2-METHYLPROPANOL(CAS DataBase Reference)
• NIST Chemistry Reference: FMOC-2-AMINO-2-METHYLPROPANOL(1187667-02-2)
• EPA Substance Registry System: FMOC-2-AMINO-2-METHYLPROPANOL(1187667-02-2)

Safety Data

• Hazardous Substances Data: 1187667-02-2(Hazardous Substances Data)

Usage

Description

FMOC-2-AMINO-2-METHYLPROPANOL, with the chemical formula C17H19NO3, is a derivative of 2-amino-2-methyl-1-propanol. It is a versatile chemical compound widely used in the field of organic chemistry, particularly for its role as a protecting group for amino acids in organic synthesis. The FMOC group acts as a temporary shield for the amine group, preventing unwanted reactions during the synthesis process.

Uses

Used in Organic Synthesis:
FMOC-2-AMINO-2-METHYLPROPANOL is used as a protecting group for amino acids, serving to shield the amine group and prevent unwanted reactions during the synthesis process. This application is crucial for maintaining the integrity and functionality of the amino acids in various chemical reactions.
Used in Peptide Synthesis:
In the field of peptide synthesis, FMOC-2-AMINO-2-METHYLPROPANOL is employed as a protecting agent for the amine group of amino acids. This protection allows for the controlled stepwise assembly of peptide chains, facilitating the synthesis of complex peptide structures with specific functions and properties.
Used in Biochemical Applications:
FMOC-2-AMINO-2-METHYLPROPANOL is also utilized in various biochemical applications, where its ability to protect the amine group of amino acids is essential for the successful execution of experiments and the development of new biochemical techniques and products.

Downstream Products

• 1187667-21-5 (9H-fluoren-9-yl)methyl 1-(4-methoxybenzyloxy)-2-methylpropan-2-ylcarbamate