6-Chloro-1-naphthoic acid

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Reagent Code: #129687
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CAS Number 16650-53-6

science Other reagents with same CAS 16650-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.63 g/mol
Formula C₁₁H₇ClO₂
badge Registry Numbers
MDL Number MFCD11848487
thermostat Physical Properties
Melting Point 188-189 °C
Boiling Point 400.6±18.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.395±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of dyes and pigments, particularly for producing naphthoic acid derivatives that contribute to color stability and lightfastness. Employed in the development of agrochemicals, serving as a building block for herbicides and plant growth regulators due to its ability to influence auxin-like activity. Also utilized in research for preparing fluorescent probes and organic semiconductors, where its aromatic structure supports electron delocalization and enhances photophysical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿21,750.00

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6-Chloro-1-naphthoic acid
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Used as a key intermediate in the synthesis of dyes and pigments, particularly for producing naphthoic acid derivatives that contribute to color stability and lightfastness. Employed in the development of agrochemicals, serving as a building block for herbicides and plant growth regulators due to its ability to influence auxin-like activity. Also utilized in research for preparing fluorescent probes and organic semiconductors, where its aromatic structure supports electron delocalization and enhances photop
Used as a key intermediate in the synthesis of dyes and pigments, particularly for producing naphthoic acid derivatives that contribute to color stability and lightfastness. Employed in the development of agrochemicals, serving as a building block for herbicides and plant growth regulators due to its ability to influence auxin-like activity. Also utilized in research for preparing fluorescent probes and organic semiconductors, where its aromatic structure supports electron delocalization and enhances photophysical properties.
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