Methyl 4-(oxazol-5-yl)benzoate

98%

Reagent Code: #205616
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CAS Number 179057-14-8

science Other reagents with same CAS 179057-14-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.20 g/mol
Formula C₁₁H₉NO₃
badge Registry Numbers
MDL Number MFCD03012557
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure, featuring a methyl benzoate with an oxazol-5-yl substituent, allows functionalization for building complex molecules, particularly in the development of bioactive compounds such as antimicrobial, anti-inflammatory, and anticancer agents. Commonly employed in cross-coupling reactions and multicomponent reactions due to the presence of aromatic and heterocyclic rings. Also explored in materials science for designing specialty polymers and luminescent compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿450.00
1g
10-20 days ฿1,750.00
5g
10-20 days ฿8,480.00
25g
10-20 days ฿41,250.00
Methyl 4-(oxazol-5-yl)benzoate
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure, featuring a methyl benzoate with an oxazol-5-yl substituent, allows functionalization for building complex molecules, particularly in the development of bioactive compounds such as antimicrobial, anti-inflammatory, and anticancer agents. Commonly employed in cross-coupling reactions and multicomponent reactions due to the presence of aromatic and heterocyclic rings. Also explored in materials science for de

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Its structure, featuring a methyl benzoate with an oxazol-5-yl substituent, allows functionalization for building complex molecules, particularly in the development of bioactive compounds such as antimicrobial, anti-inflammatory, and anticancer agents. Commonly employed in cross-coupling reactions and multicomponent reactions due to the presence of aromatic and heterocyclic rings. Also explored in materials science for designing specialty polymers and luminescent compounds.

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