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(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride

  • CAS No. 201009-98-5

  • Cat. No. CS-0150968
  • Purity≥95%
  • MDL No.MFCD00153447

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

(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride|CS-0150968

Structure of 201009-98-5

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General Information

  • CAS No. 201009-98-5
  • Cat. No. CS-0150968
  • Purity ≥95%
  • MDL No. MFCD00153447
  • Storage 4°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₂H₂₇ClN₂O₄
  • Molecular Weight 418.91
  • Synonym(s) N'-Fmoc-L-lysine methyl ester hydrochloride
  • SMILES COC([C@@H](N)CCCCNC(OCC1C2=CC=CC=C2C3=CC=CC=C31)=O)=O.Cl

Description

(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride is a chiral, bench-stable amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group. This compound integrates seamlessly into solid-phase peptide synthesis workflows, enabling efficient N-terminal protection and selective coupling reactions under standard conditions.

Application

(S)-Methyl 6-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoate hydrochloride serves as a protected amino acid building block for peptide synthesis, enabling efficient N-terminal capping and side-chain compatibility. The Fmoc group ensures orthogonal deprotection under mild basic conditions, while the methyl ester facilitates straightforward conversion to carboxylic acids or amides. Bench-stable and readily purified by chromatography, it functions reliably in solid-phase and solution-phase workflows.

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   90.65
  • LogP   3.6175
  • H_Acceptors   5
  • H_Donors   2
  • Rotatable_Bonds   8

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