Ethyl thiazole-4-carboxylate

≥95%

Reagent Code: #181922
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CAS Number 14527-43-6

science Other reagents with same CAS 14527-43-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.19 g/mol
Formula C₆H₇NO₂S
badge Registry Numbers
MDL Number MFCD03788566
thermostat Physical Properties
Melting Point 51-55 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of thiazole-based drugs with antimicrobial and anti-inflammatory properties. Commonly employed in research for developing new bioactive compounds due to the thiazole ring’s prevalence in medicinal chemistry. Also utilized in agrochemicals for crop protection agents, leveraging its reactivity in heterocyclic transformations. Serves as a building block in organic synthesis, especially in cross-coupling and ester hydrolysis reactions to generate functionalized thiazoles.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿1,060.00
inventory 25g
10-20 days ฿4,100.00
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Ethyl thiazole-4-carboxylate
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Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of thiazole-based drugs with antimicrobial and anti-inflammatory properties. Commonly employed in research for developing new bioactive compounds due to the thiazole ring’s prevalence in medicinal chemistry. Also utilized in agrochemicals for crop protection agents, leveraging its reactivity in heterocyclic transformations. Serves as a building block in organic synthesis, especially in cross-coupling and ester hyd

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of thiazole-based drugs with antimicrobial and anti-inflammatory properties. Commonly employed in research for developing new bioactive compounds due to the thiazole ring’s prevalence in medicinal chemistry. Also utilized in agrochemicals for crop protection agents, leveraging its reactivity in heterocyclic transformations. Serves as a building block in organic synthesis, especially in cross-coupling and ester hydrolysis reactions to generate functionalized thiazoles.

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