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Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc

  • CAS No. 894096-02-7

  • Cat. No. CS-0128271
  • Purity≥98%
  • MDL No.MFCD34470435

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

Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc|CS-0128271

Structure of 894096-02-7

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General Information

  • CAS No. 894096-02-7
  • Cat. No. CS-0128271
  • Purity ≥98%
  • MDL No. MFCD34470435
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₃₈H₄₀N₂O₁₄
  • Molecular Weight 748.73
  • Synonym(s) None
  • SMILES O=C(OC)[C@@H](O1)[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC2=CC=C(CO)C=C2NC(CCNC(OCC3C4=C(C5=C3C=CC=C5)C=CC=C4)=O)=O

Description

Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc features a protected glucuronic acid scaffold with a benzyl alcohol handle and Fmoc-blocking group, enabling direct conjugation in glycochemistry workflows. This stable, moisture-tolerant derivative simplifies the synthesis of complex glycoconjugates and oligosaccharide libraries under standard conditions.

Application

Me-triacetyl-β-D-glucopyranuronate-Ph-CH2OH-Fmoc serves as a versatile glycosyl building block for the synthesis of complex oligosaccharides and glycoconjugates. The triacetylated glucuronic acid moiety provides enhanced stability and facilitates selective deprotection, while the Fmoc-protected benzyl alcohol functionality enables orthogonal coupling in solid-phase glycosylation workflows. This construct supports efficient C-glycoside formation and is compatible with standard peptide and carbohydrate coupling protocols.

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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   211.32
  • LogP   3.118
  • H_Acceptors   14
  • H_Donors   3
  • Rotatable_Bonds   13

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