Ethyl 2-(4-ethylphenyl)thiazole-4-carboxylate

≥95%

Reagent Code: #181925
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CAS Number 885278-69-3

science Other reagents with same CAS 885278-69-3

blur_circular Chemical Specifications

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Weight 261.34 g/mol
Formula C₁₄H₁₅NO₂S
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MDL Number MFCD06738347
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of novel thiazole-based drugs due to its favorable reactivity and structural compatibility with bioactive molecules. Also employed in agrochemical research for designing new crop protection agents owing to its stability and functional group tolerance. Its ester functionality allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,540.00
inventory 1g
10-20 days ฿24,220.00
inventory 250mg
10-20 days ฿7,510.00

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Ethyl 2-(4-ethylphenyl)thiazole-4-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of novel thiazole-based drugs due to its favorable reactivity and structural compatibility with bioactive molecules. Also employed in agrochemical research for designing new crop protection agents owing to its stability and functional group tolerance. Its ester functionality allows for easy modification, mak

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of novel thiazole-based drugs due to its favorable reactivity and structural compatibility with bioactive molecules. Also employed in agrochemical research for designing new crop protection agents owing to its stability and functional group tolerance. Its ester functionality allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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