1211504-14-1

Basic information

• Product Name: N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid
• Synonyms: N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid;2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(pent-4-en-1-yl)dec-9-enoic acid
• CAS NO: 1211504-14-1
• Molecular Formula: C30H37NO4
• Molecular Weight: 475.61908
• Mol File: 1211504-14-1.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 637.4±55.0 °C at 760 mmHg
• Flash Point: 339.3±31.5 °C
• Appearance: /
• Density: 1.104
• Storage Temp.: 2-8°C
• CAS DataBase Reference: N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid(1211504-14-1)
• EPA Substance Registry System: N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid(1211504-14-1)

Safety Data

• Hazardous Substances Data: 1211504-14-1(Hazardous Substances Data)

Usage

General Description

N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid is a chemical compound used in the synthesis of peptides. It consists of a 2-amino-2-(pent-4-enyl)dec-9-enoic acid unit with a N-Fmoc (9-fluorenylmethoxycarbonyl) protecting group attached to the amino group. N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid is valuable in peptide synthesis as it can be used as a building block for the assembly of complex peptide structures. It is commonly employed in the solid-phase peptide synthesis process, where the N-Fmoc group can be selectively removed to expose the amino group for further coupling reactions. Overall, N-Fmoc-2-amino-2-(pent-4-enyl)dec-9-enoic acid plays a crucial role in the production of custom peptides for various research and industrial applications.