5'-Chloro-3-hydroxy-2',4'-dimethoxy-2-naphthanilide

98%

Reagent Code: #161290
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CAS Number 92-72-8

science Other reagents with same CAS 92-72-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 357.79 g/mol
Formula C₁₉H₁₆ClNO₄
badge Registry Numbers
MDL Number MFCD00021635
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of azo dyes and pigments, this compound contributes to the production of high-performance colorants valued for their thermal stability and lightfastness. It is especially useful in the development of yellow to red shades for coatings, plastics, and textile applications. Its structure supports strong chromophoric properties, making it suitable for specialty dyes in inkjet printing and automotive finishes. Additionally, it has been explored in the formulation of optical brighteners and fluorescent probes due to its conjugated aromatic system and substitution pattern favorable for electron delocalization.

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Test Parameter Specification
Appearance White to Amber powder to crystal
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿258.00
inventory 5g
10-20 days ฿1,660.00

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5'-Chloro-3-hydroxy-2',4'-dimethoxy-2-naphthanilide
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Used primarily as an intermediate in the synthesis of azo dyes and pigments, this compound contributes to the production of high-performance colorants valued for their thermal stability and lightfastness. It is especially useful in the development of yellow to red shades for coatings, plastics, and textile applications. Its structure supports strong chromophoric properties, making it suitable for specialty dyes in inkjet printing and automotive finishes. Additionally, it has been explored in the formulat

Used primarily as an intermediate in the synthesis of azo dyes and pigments, this compound contributes to the production of high-performance colorants valued for their thermal stability and lightfastness. It is especially useful in the development of yellow to red shades for coatings, plastics, and textile applications. Its structure supports strong chromophoric properties, making it suitable for specialty dyes in inkjet printing and automotive finishes. Additionally, it has been explored in the formulation of optical brighteners and fluorescent probes due to its conjugated aromatic system and substitution pattern favorable for electron delocalization.

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