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Methyl 2-aminooxazole-5-carboxylate

  • CAS No. 934236-40-5

  • Cat. No. CS-0130344
  • Purity≥96%
  • MDL No.MFCD09265526

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

Methyl 2-aminooxazole-5-carboxylate|CS-0130344

Structure of 934236-40-5

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General Information

  • CAS No. 934236-40-5
  • Cat. No. CS-0130344
  • Purity ≥96%
  • MDL No. MFCD09265526
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₆N₂O₃
  • Molecular Weight 142.11
  • Synonym(s) Methyl 2-amino-1,3-oxazole-5-carboxylate
  • SMILES O=C(OC)C1=CN=C(O1)N

Description

Methyl 2-aminooxazole-5-carboxylate features a polar oxazole ring fused with an electron-rich amine and ester functionality, enabling seamless integration into heterocyclic scaffolds. This bench-stable derivative supports direct coupling in synthetic sequences and serves as a key intermediate for bioactive molecule construction.

Application

Methyl 2-aminooxazole-5-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to oxazole-based scaffolds prevalent in medicinal chemistry. The molecule combines a reactive amine and ester functional group, facilitating diverse transformations including nucleophilic substitution, coupling reactions, and cyclization processes. Its bench-stable nature and compatibility with standard purification techniques make it well-suited for iterative synthetic workflows and API intermediate development.

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   78.35
  • LogP   0.0434
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   1

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