Ethyl 2,4-Dimethylthiazole-5-Carboxylate

≥97%

Reagent Code: #182971
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CAS Number 7210-77-7

science Other reagents with same CAS 7210-77-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.24 g/mol
Formula C₈H₁₁NO₂S
badge Registry Numbers
MDL Number MFCD00052874
thermostat Physical Properties
Melting Point 48-50 °C
Boiling Point 254.3ºC
inventory_2 Storage & Handling
Density 1.164 g/cm3
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs which exhibit antimicrobial, anti-inflammatory, and antitumor activities. It serves as a building block in medicinal chemistry due to the presence of the functionalized thiazole ring, which is common in bioactive molecules. Its ester group allows for easy modification, enabling the preparation of diverse derivatives for structure-activity relationship studies. Also employed in agrochemical research for designing novel pesticides and fungicides, leveraging the thiazole scaffold’s stability and biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,700.00
inventory 10g
10-20 days ฿3,360.00
inventory 25g
10-20 days ฿8,150.00
inventory 100g
10-20 days ฿26,780.00

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Ethyl 2,4-Dimethylthiazole-5-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs which exhibit antimicrobial, anti-inflammatory, and antitumor activities. It serves as a building block in medicinal chemistry due to the presence of the functionalized thiazole ring, which is common in bioactive molecules. Its ester group allows for easy modification, enabling the preparation of diverse derivatives for structure-activity relationship studies. Also employed in agrochemi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of thiazole-based drugs which exhibit antimicrobial, anti-inflammatory, and antitumor activities. It serves as a building block in medicinal chemistry due to the presence of the functionalized thiazole ring, which is common in bioactive molecules. Its ester group allows for easy modification, enabling the preparation of diverse derivatives for structure-activity relationship studies. Also employed in agrochemical research for designing novel pesticides and fungicides, leveraging the thiazole scaffold’s stability and biological activity.

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