5-Methoxy-2-methylbenzoxazole

98%

Reagent Code: #205276
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CAS Number 5676-57-3

science Other reagents with same CAS 5676-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.18 g/mol
Formula C₉H₉NO₂
badge Registry Numbers
MDL Number MFCD00128831
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of bioactive molecules due to the benzoxazole core, which is known for its stability and biological activity. Commonly employed in the preparation of fluorescent dyes and optical brighteners because of its electron-rich structure that enhances light absorption and emission. Also explored in medicinal chemistry for potential antimicrobial and anti-inflammatory agents. Its methoxy and methyl substituents improve lipophilicity, aiding in cell membrane penetration for drug design applications.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿55,000.00
5-Methoxy-2-methylbenzoxazole
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of bioactive molecules due to the benzoxazole core, which is known for its stability and biological activity. Commonly employed in the preparation of fluorescent dyes and optical brighteners because of its electron-rich structure that enhances light absorption and emission. Also explored in medicinal chemistry for potential antimicrobial and anti-inflammatory agents. Its metho

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Serves as a building block in the development of bioactive molecules due to the benzoxazole core, which is known for its stability and biological activity. Commonly employed in the preparation of fluorescent dyes and optical brighteners because of its electron-rich structure that enhances light absorption and emission. Also explored in medicinal chemistry for potential antimicrobial and anti-inflammatory agents. Its methoxy and methyl substituents improve lipophilicity, aiding in cell membrane penetration for drug design applications.

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