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Ethyl 2-chloro-1,3-oxazole-5-carboxylate

  • CAS No. 862599-47-1

  • Cat. No. CS-D0874
  • Purity≥95%
  • MDL No.MFCD09475866

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

Ethyl 2-chloro-1,3-oxazole-5-carboxylate|CS-D0874

Structure of 862599-47-1

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General Information

  • CAS No. 862599-47-1
  • Cat. No. CS-D0874
  • Purity ≥95%
  • MDL No. MFCD09475866
  • Storage -20°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₆ClNO₃
  • Molecular Weight None
  • Synonym(s) Ethyl 2-chlorooxazole-5-carboxylate
  • SMILES O=C(OCC)C1=CN=C(Cl)O1

Description

Ethyl 2-chloro-1,3-oxazole-5-carboxylate features a chlorinated oxazole ring that imparts enhanced electrophilicity and stability under standard conditions. This heterocyclic ester integrates readily into synthetic sequences requiring selective reactivity at the 2-position, serving as a key intermediate in the construction of functionalized oxazoles and bioactive molecules.

Application

Ethyl 2-chloro-1,3-oxazole-5-carboxylate serves as a versatile heterocyclic building block for the synthesis of oxazole-based pharmaceuticals and agrochemicals. The electron-deficient oxazole ring enables efficient nucleophilic substitution at the C2 position, while the ester functionality supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with standard coupling reactions facilitate straightforward integration into complex molecular architectures.

Synthesis

  • Route1

    References

    • Organic Letters, , vol. 7, # 15 p. 3351 - 3354

Safety Information

Download SDS
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   52.33
  • LogP   1.5047
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   2

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