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(9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate

  • CAS No. 205688-13-7

  • Cat. No. CS-0155936
  • Purity≥96%
  • MDL No.MFCD12912141

*For research and further manufacturing use only, not for direct human use.

(9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate|CS-0155936

Structure of 205688-13-7

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General Information

  • CAS No. 205688-13-7
  • Cat. No. CS-0155936
  • Purity ≥96%
  • MDL No. MFCD12912141
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₁₈N₂O₂
  • Molecular Weight 330.38
  • Synonym(s) N-(4-aminophenyl)-Carbamic acid9H-fluoren-9-ylmethyl ester
  • SMILES C1=CC=C2C(=C1)C3=CC=CC=C3C2COC(=O)NC4=CC=C(C=C4)N

Description

This fluorenylmethoxy carbamate derivative features a robust protecting group for primary amines, combining the stability of the 9-fluorenylmethyl (Fmoc) moiety with a para-aminophenyl linker. The carbamate linkage enables efficient deprotection under mild basic conditions, facilitating controlled release during peptide synthesis and enabling clean coupling reactions in biopharmaceutical workflows.

Application

(9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate serves as a robust amino-protecting group for peptide synthesis and nucleoside derivatization. Its fluorenylmethoxycarbonyl (Fmoc) moiety enables orthogonal deprotection under mild basic conditions, while the para-aminophenyl carbamate functionality offers enhanced stability and compatibility with diverse functional groups. This compound facilitates efficient solid-phase synthesis and simplifies purification through distinct chromatographic behavior.

Synthesis

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    • In-stock
      (9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate|CS-0155936
      205688-13-7

    References

    • WO2009/37229 A1, ; Page/Page column 28 ;

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

Quality Control

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Computational Chemistry Data

  • TPSA   64.35
  • LogP   4.6298
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   3

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