Methyl 2-(2-aminothiazol-5-yl)acetate

Name: Methyl 2-(2-aminothiazol-5-yl)acetate
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CAS No. 110295-93-7
Cat. No. CS-0053534
Purity≥97%
MDL No.None

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Methyl 2-(2-aminothiazol-5-yl)acetate|CS-0053534

Structure of 110295-93-7

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General Information

CAS No. 110295-93-7
Cat. No. CS-0053534
Purity ≥97%
MDL No. None
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₆H₈N₂O₂S
Molecular Weight 172.20
Synonym(s) (2-Amino-thiazol-5-yl)-acetic acid methyl ester
SMILES COC(=O)CC1=CN=C(N)S1

Description

Methyl 2-(2-aminothiazol-5-yl)acetate features a reactive thiazole scaffold with a pendant amino group and ester functionality, enabling direct incorporation into diverse heterocyclic architectures. This bench-stable reagent facilitates efficient coupling reactions in medicinal chemistry and combinatorial synthesis workflows.

Application

Methyl 2-(2-aminothiazol-5-yl)acetate serves as a versatile building block in medicinal chemistry, enabling efficient access to thiazole-containing scaffolds. The molecule combines a reactive thiazole ring with an α-aminoester functionality, facilitating diverse transformations including nucleophilic substitutions, amidations, and metal-catalyzed couplings. Its bench-stable nature and straightforward purification make it well-suited for iterative synthesis campaigns targeting bioactive heterocycles.

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 0.4408
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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Methyl 2-(2-aminothiazol-5-yl)acetate

CAS No. 110295-93-7

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