1172579-62-2

Basic information

• Product Name: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid
• Synonyms: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid
• CAS NO: 1172579-62-2
• Molecular Formula: C₂₂H₂₅NO₄
• Molecular Weight: 367.4382
• Mol File: 1172579-62-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 532.0±29.0 °C(Predicted)
• Appearance: /
• Density: 1.195±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 3.94±0.10(Predicted)
• CAS DataBase Reference: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid(1172579-62-2)
• EPA Substance Registry System: (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid(1172579-62-2)

Safety Data

• Hazardous Substances Data: 1172579-62-2(Hazardous Substances Data)

Usage

General Description

The chemical, also known as Fmoc-D-Leucine, is a derivative of the amino acid leucine. It is commonly used in organic chemistry and peptide synthesis as a protecting group for the amine functionality of amino acids. The Fmoc protecting group can be selectively removed under mild basic conditions, allowing for the stepwise synthesis of peptides and small proteins. (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3,3-dimethylbutanoic acid is often used in the development of new pharmaceuticals, as well as in the study of protein structure and function.