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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)butanoic acid

  • CAS No. 235788-61-1

  • Cat. No. CS-0047631
  • Purity≥95%
  • MDL No.MFCD11111552

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

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)butanoic acid|CS-0047631

Structure of 235788-61-1

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General Information

  • CAS No. 235788-61-1
  • Cat. No. CS-0047631
  • Purity ≥95%
  • MDL No. MFCD11111552
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₉H₃₂N₂O₆
  • Molecular Weight 504.57
  • Synonym(s) FMOC-L-DAB(DDE)-OH
  • SMILES O=C(O)[C@@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CCN/C(C)=C4C(CC(C)(C)CC/4=O)=O

Description

This (S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)butanoic acid features a fluorenylmethoxycarbonyl (Fmoc) group for controlled peptide synthesis and a sterically hindered side chain with a diketone functionality, enabling selective coupling under standard conditions.

Application

(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)ethyl)amino)butanoic acid serves as a robust chiral building block for peptide synthesis, leveraging the Fmoc group for orthogonal protection and enabling efficient coupling under standard conditions. The pendant cyclohexanedione-derived amine moiety provides a versatile handle for downstream functionalization, while the molecule exhibits excellent bench stability and compatibility with common purification methods.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H312-H315-H319
Precautionary Statements : P261-P280-P302+P352

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Computational Chemistry Data

  • TPSA   121.8
  • LogP   4.1902
  • H_Acceptors   6
  • H_Donors   3
  • Rotatable_Bonds   8

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