Ethyl thiazole-5-carboxylate

≥95%

Reagent Code: #181950
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CAS Number 32955-22-9

science Other reagents with same CAS 32955-22-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.19 g/mol
Formula C₆H₇NO₂S
badge Registry Numbers
MDL Number MFCD06205069
thermostat Physical Properties
Boiling Point 235.7 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.242±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial, anti-inflammatory, and antidiabetic properties. Commonly employed in organic synthesis to introduce the thiazole ring system into larger molecules. Also utilized in the preparation of agrochemicals and bioactive compounds due to its ability to enhance metabolic stability and binding affinity in lead compounds. Frequently applied in research settings for the design of novel heterocyclic compounds with potential therapeutic activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,500.00
inventory 10g
10-20 days ฿2,210.00
inventory 25g
10-20 days ฿5,500.00
inventory 100g
10-20 days ฿21,990.00
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Ethyl thiazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial, anti-inflammatory, and antidiabetic properties. Commonly employed in organic synthesis to introduce the thiazole ring system into larger molecules. Also utilized in the preparation of agrochemicals and bioactive compounds due to its ability to enhance metabolic stability and binding affinity in lead compounds. Frequently applied in research settings for the design of

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs with antimicrobial, anti-inflammatory, and antidiabetic properties. Commonly employed in organic synthesis to introduce the thiazole ring system into larger molecules. Also utilized in the preparation of agrochemicals and bioactive compounds due to its ability to enhance metabolic stability and binding affinity in lead compounds. Frequently applied in research settings for the design of novel heterocyclic compounds with potential therapeutic activity.

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