3-Hydroxy-2-naphthoic Acid 2-Chloroanilide

≥98%(T)

Reagent Code: #195036
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CAS Number 6704-40-1

science Other reagents with same CAS 6704-40-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.74 g/mol
Formula C₁₇H₁₂ClNO₂
badge Registry Numbers
MDL Number MFCD00191652
thermostat Physical Properties
Melting Point 228°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of naphthopyranone-based dyes and pigments, particularly for high-performance colorants in coatings and inks. It plays a key role in forming complex heterocyclic structures valued for their thermal stability and colorfastness. Also employed in the development of photochromic materials, where it contributes to light-responsive properties in specialty applications like ophthalmic lenses and smart windows. Its chloroanilide functionality enhances reactivity in coupling reactions, making it useful in fine chemical synthesis for agrochemicals and pharmaceuticals.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿374.00
1g
10-20 days ฿1,474.00
3-Hydroxy-2-naphthoic Acid 2-Chloroanilide
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Used as an intermediate in the synthesis of naphthopyranone-based dyes and pigments, particularly for high-performance colorants in coatings and inks. It plays a key role in forming complex heterocyclic structures valued for their thermal stability and colorfastness. Also employed in the development of photochromic materials, where it contributes to light-responsive properties in specialty applications like ophthalmic lenses and smart windows. Its chloroanilide functionality enhances reactivity in coupli

Used as an intermediate in the synthesis of naphthopyranone-based dyes and pigments, particularly for high-performance colorants in coatings and inks. It plays a key role in forming complex heterocyclic structures valued for their thermal stability and colorfastness. Also employed in the development of photochromic materials, where it contributes to light-responsive properties in specialty applications like ophthalmic lenses and smart windows. Its chloroanilide functionality enhances reactivity in coupling reactions, making it useful in fine chemical synthesis for agrochemicals and pharmaceuticals.

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