Methyl 3-methoxy-1-naphthoate

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Reagent Code: #203465
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CAS Number 33295-56-6

science Other reagents with same CAS 33295-56-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.23 g/mol
Formula C₁₃H₁₂O₃
badge Registry Numbers
MDL Number MFCD18413142
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of naphthoquinone-based compounds with potential biological activity. Its structure allows for further functionalization in organic reactions, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent dyes and optical brighteners due to the naphthalene core's inherent photophysical properties. Commonly utilized in academic and industrial labs for building complex polycyclic molecules through ester hydrolysis, ether cleavage, or cross-coupling reactions.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿34,470.00
inventory 100mg
10-20 days ฿58,590.00
inventory 250mg
10-20 days ฿99,590.00
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Methyl 3-methoxy-1-naphthoate
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Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of naphthoquinone-based compounds with potential biological activity. Its structure allows for further functionalization in organic reactions, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent dyes and optical brighteners due to the naphthalene core's inherent photophysical properties. Commonly utilized in academic and industrial labs for bui

Used as a key intermediate in the synthesis of pharmaceuticals and fine chemicals, particularly in the development of naphthoquinone-based compounds with potential biological activity. Its structure allows for further functionalization in organic reactions, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent dyes and optical brighteners due to the naphthalene core's inherent photophysical properties. Commonly utilized in academic and industrial labs for building complex polycyclic molecules through ester hydrolysis, ether cleavage, or cross-coupling reactions.

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