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ethyl 4-amino-2-methyl-1,3-thiazole-5-carboxylate

  • CAS No. 278183-12-3

  • Cat. No. CS-0038043
  • Purity≥97%
  • MDL No.MFCD20719055

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

ethyl 4-amino-2-methyl-1,3-thiazole-5-carboxylate|CS-0038043

Structure of 278183-12-3

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General Information

  • CAS No. 278183-12-3
  • Cat. No. CS-0038043
  • Purity ≥97%
  • MDL No. MFCD20719055
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₁₀N₂O₂S
  • Molecular Weight 186.23
  • Synonym(s) ethyl 4-amino-2-methylthiazole-5-carboxylate
  • SMILES CCOC(=O)C1=C(N)N=C(C)S1

Description

Ethyl 4-amino-2-methyl-1,3-thiazole-5-carboxylate features a bifunctional thiazole scaffold with an electron-rich amino group and a sterically accessible methyl substituent. This bench-stable derivative integrates readily into heterocyclic synthesis, enabling efficient access to bioactive analogs through nucleophilic substitution or coupling reactions under standard conditions.

Application

Ethyl 4-amino-2-methyl-1,3-thiazole-5-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to substituted thiazoles via standard functional group transformations. Its amino and ester groups offer orthogonal reactivity for coupling, cyclization, and derivatization, facilitating the synthesis of heterocyclic scaffolds relevant to pharmaceutical research. The compound exhibits good bench stability and is amenable to purification by standard chromatographic methods, supporting scalable synthesis 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-P330-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   65.21
  • LogP   1.21042
  • H_Acceptors   5
  • H_Donors   1
  • Rotatable_Bonds   2

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