2-Methyl-1,3-benzoxazole-6-carboxylic acid

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Reagent Code: #206120
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CAS Number 13452-14-7

science Other reagents with same CAS 13452-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.16 g/mol
Formula C₉H₇NO₃
badge Registry Numbers
MDL Number MFCD07787266
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with potential antimicrobial, anti-inflammatory, or antitumor properties. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex benzoxazole derivatives. It is also employed in research for designing fluorescent probes and optoelectronic materials due to the inherent photophysical properties of the benzoxazole core. Additionally, derivatives of this compound are explored in medicinal chemistry for their enzyme inhibitory activities.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,090.00
inventory 5g
10-20 days ฿8,490.00

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2-Methyl-1,3-benzoxazole-6-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with potential antimicrobial, anti-inflammatory, or antitumor properties. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex benzoxazole derivatives. It is also employed in research for designing fluorescent probes and optoelectronic materials due to the inherent photophysical properties of the benzoxazole core. Additi

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with potential antimicrobial, anti-inflammatory, or antitumor properties. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex benzoxazole derivatives. It is also employed in research for designing fluorescent probes and optoelectronic materials due to the inherent photophysical properties of the benzoxazole core. Additionally, derivatives of this compound are explored in medicinal chemistry for their enzyme inhibitory activities.

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