307531-88-0

Basic information

• Product Name: (S)-(+)-N-BOC-3-N-FMOC-AMINOPYRROLIDINE&
• Synonyms: (S)-1-BOC-3-FMOC-AMINOPYRROLIDINE;(S)-N-BOC-3-FMOC-AMINOPYRROLIDINE;(S)-tert-Butyl 3-((((9H-fluoren-9-yl)methoxy)-carbonyl)amino)pyrrolidine-1-carboxylate
• CAS NO: 307531-88-0
• Molecular Formula: C24H28N2O4
• Molecular Weight: 408.49012
• Mol File: 307531-88-0.mol
• Article Data: 0

Chemical Properties

• Melting Point: 172-180 °C (DSC)
• Boiling Point: 567.2 °C at 760 mmHg
• Flash Point: 296.8 °C
• Appearance: /
• Density: 1.24 g/cm³
• Vapor Pressure: 7E-13mmHg at 25°C
• Refractive Index: 1.61
• Storage Temp.: ?20°C
• CAS DataBase Reference: (S)-(+)-N-BOC-3-N-FMOC-AMINOPYRROLIDINE&(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-(+)-N-BOC-3-N-FMOC-AMINOPYRROLIDINE&(307531-88-0)
• EPA Substance Registry System: (S)-(+)-N-BOC-3-N-FMOC-AMINOPYRROLIDINE&(307531-88-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 307531-88-0(Hazardous Substances Data)

Usage

General Description

(S)-(+)-N-BOC-3-N-FMOC-AMINOPYRROLIDINE is a chemical compound used primarily in organic synthesis and medicinal chemistry. It is a derivative of aminopyrrolidine that has a BOC (tert-butoxycarbonyl) protecting group on the nitrogen atom and an FMOC (9-fluorenylmethoxycarbonyl) protecting group on the 3-position of the pyrrolidine ring. These protecting groups are used to protect specific functional groups during chemical reactions and can be removed under mild conditions to reveal the desired functional groups. (S)-(+)-N-BOC-3-N-FMOC-AMINOPYRROLIDINE& is often used as a building block in the synthesis of various pharmaceuticals and bioactive compounds due to its stability and reactivity.

InChI:InChI=1/C24H28N2O4/c1-24(2,3)30-23(28)26-13-12-16(14-26)25-22(27)29-15-21-19-10-6-4-8-17(19)18-9-5-7-11-20(18)21/h4-11,16,21H,12-15H2,1-3H3,(H,25,27)/t16-/m0/s1