Ethyl 4-methyloxazole-2-carboxylate

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Reagent Code: #184313
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CAS Number 90892-99-2

science Other reagents with same CAS 90892-99-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 155.15 g/mol
Formula C₇H₉NO₃
badge Registry Numbers
MDL Number MFCD09038239
thermostat Physical Properties
Boiling Point 218 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its structure supports the construction of heterocyclic compounds that are active in biological systems. Commonly employed in medicinal chemistry for building blocks in drug design, especially in the preparation of oxazole-based bioactive molecules. Also utilized in agrochemical research for developing new crop protection agents due to its reactivity and stability in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,080.00
inventory 250mg
10-20 days ฿5,840.00
inventory 1g
10-20 days ฿17,380.00
inventory 5g
10-20 days ฿85,430.00
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Ethyl 4-methyloxazole-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its structure supports the construction of heterocyclic compounds that are active in biological systems. Commonly employed in medicinal chemistry for building blocks in drug design, especially in the preparation of oxazole-based bioactive molecules. Also utilized in agrochemical research for developing new crop protection agents due to its reactivity and stability in synthet
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiviral and antibacterial agents. Its structure supports the construction of heterocyclic compounds that are active in biological systems. Commonly employed in medicinal chemistry for building blocks in drug design, especially in the preparation of oxazole-based bioactive molecules. Also utilized in agrochemical research for developing new crop protection agents due to its reactivity and stability in synthetic pathways.
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