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CS-W001157 4
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[5-(2-Thienyl)-3-isoxazolyl]methanol

  • CAS No. 194491-44-6

  • Cat. No. CS-0073743
  • Purity≥98%
  • MDL No.MFCD03086162

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

[5-(2-Thienyl)-3-isoxazolyl]methanol|CS-0073743

Structure of 194491-44-6

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General Information

  • CAS No. 194491-44-6
  • Cat. No. CS-0073743
  • Purity ≥98%
  • MDL No. MFCD03086162
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇NO₂S
  • Molecular Weight 181.21
  • Synonym(s) None
  • SMILES OCC1=NOC(C2=CC=CS2)=C1

Description

This boronate moiety integrates a 5-(2-thienyl)-3-isoxazolyl group with a terminal alcohol, enabling efficient coupling in cross-coupling reactions. The thiophene isolevelling electron density enhances reactivity, while the isoxazole ring provides stability under standard conditions.

Application

[5-(2-Thienyl)-3-isoxazolyl]methanol serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its isoxazole ring fused with a thienyl moiety provides enhanced electronic delocalization and metabolic stability. The pendant primary alcohol facilitates straightforward derivatization—via oxidation, protection, or coupling reactions—while maintaining excellent bench stability and compatibility with standard synthetic 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

Quality Control

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Computational Chemistry Data

  • TPSA   46.26
  • LogP   1.8954
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   2

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