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CS-W001157 4
Total: USD 88.00

Ketoconazole impurity 6

  • CAS No. 134071-44-6

  • Cat. No. CS-0186098
  • Purity≥98%
  • MDL No.MFCD07367827

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

Ketoconazole impurity 6|CS-0186098

Structure of 134071-44-6

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General Information

  • CAS No. 134071-44-6
  • Cat. No. CS-0186098
  • Purity ≥98%
  • MDL No. MFCD07367827
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₂₁H₂₀Cl₂N₂O₅S
  • Molecular Weight 483.36
  • Synonym(s) None
  • SMILES C([C@]1(O[C@@H](COS(=O)(=O)C2=CC=C(C)C=C2)CO1)C3=C(Cl)C=C(Cl)C=C3)N4C=CN=C4

Description

This imidazole-containing dioxolane derivative features a sterically hindered, bench-stable scaffold with enhanced solubility in polar organic media. The para-methylbenzenesulfonate group enables efficient coupling reactions under mild conditions, while the cis-configuration ensures predictable stereochemical control in asymmetric synthesis workflows.

Application

(cis-2-((1H-Imidazol-1-yl)methyl)-2-(2,4-dichlorophenyl)-1,3-dioxolan-4-yl)methyl 4-methylbenzenesulfonate serves as a stable, bench-ready glycosyl donor for stereoselective glycosylation reactions. The imidazole-bearing dioxolane scaffold enables efficient C-glycosylation under mild conditions, with the tosylate group facilitating activation via SN2 displacement. Its functional group tolerance and predictable stereocontrol make it a practical tool for constructing complex carbohydrate architectures and heterocyclic scaffolds in medicinal chemistry workflows.

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   79.65
  • LogP   4.17222
  • H_Acceptors   7
  • H_Donors   0
  • Rotatable_Bonds   7

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