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CS-W001157 4
Total: USD 88.00

(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-allothreonine

  • CAS No. 146306-75-4

  • Cat. No. CS-0100980
  • Purity≥98%
  • MDL No.MFCD01318739

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

(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-allothreonine|CS-0100980

Structure of 146306-75-4

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General Information

  • CAS No. 146306-75-4
  • Cat. No. CS-0100980
  • Purity ≥98%
  • MDL No. MFCD01318739
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₉H₁₉NO₅
  • Molecular Weight 341.36
  • Synonym(s) None
  • SMILES C[C@H](O)[C@@H](C(O)=O)NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O

Description

Fmoc-L-allothreonine is a protected amino acid derivative featuring a fluorenylmethoxycarbonyl (Fmoc) group for orthogonal protection in peptide synthesis. This configuration enables efficient N-terminal capping and facilitates purification via standard solid-phase protocols. The allothreonine side chain offers distinct stereochemical properties, enhancing structural diversity in bioactive peptide libraries.

Application

Boc-L-allothreonine, a key chiral building block in peptide synthesis, features a sterically hindered side chain and orthogonal protection for the hydroxyl group. It facilitates efficient solid-phase and solution-phase coupling reactions with excellent functional group tolerance and stability under standard deprotection conditions. The fluorenylmethoxycarbonyl (Fmoc) variant enables sequential addition in automated synthesis while maintaining high diastereoselectivity and purity.

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-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   95.86
  • LogP   2.3591
  • H_Acceptors   4
  • H_Donors   3
  • Rotatable_Bonds   5

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