Ethyl 4-aminothiazole-5-carboxylate

Name: Ethyl 4-aminothiazole-5-carboxylate
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CAS No. 152300-59-9
Cat. No. CS-W004510
Purity≥98%
MDL No.MFCD06798219

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Ethyl 4-aminothiazole-5-carboxylate|CS-W004510

Structure of 152300-59-9

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General Information

CAS No. 152300-59-9
Cat. No. CS-W004510
Purity ≥98%
MDL No. MFCD06798219
Storage 4°C, protect from light
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₆H₈N₂O₂S
Molecular Weight 172.21
Synonym(s) None
SMILES CCOC(C1=C(N=CS1)N)=O

Description

Ethyl 4-aminothiazole-5-carboxylate features a reactive thiazole core paired with an amino group and ester functionality, enabling direct incorporation into heterocyclic scaffolds. This bench-stable compound serves as a key intermediate in the synthesis of bioactive molecules, particularly within medicinal chemistry and agrochemical development workflows.

Application

Ethyl 4-aminothiazole-5-carboxylate serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-based pharmacophores. Its amino and ester functionalities offer orthogonal reactivity for diverse transformations, including amidation, alkylation, and coupling reactions. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis campaigns targeting heterocyclic APIs and functionalized scaffolds.

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 65.21
LogP 0.902
H_Acceptors 5
H_Donors 1
Rotatable_Bonds 2

Other Classifications

Building Blocks Functional Group Ester

Building Blocks Skeleton Aromatic heterocycle compounds Thiazole compounds

Key Words

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Ethyl 4-aminothiazole-5-carboxylate

CAS No. 152300-59-9

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