6-Bromo-2-naphthol

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Reagent Code: #143393
label
Alias 6-Bromo-2-hydroxynaphthalene
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CAS Number 15231-91-1

science Other reagents with same CAS 15231-91-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.07 g/mol
Formula BrC₁₀H₆OH
badge Registry Numbers
EC Number 239-279-0
MDL Number MFCD00004081
thermostat Physical Properties
Melting Point 122-124 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of dyes and fluorescent compounds due to its ability to undergo coupling reactions and halogen displacement. Commonly employed in the production of optical brighteners for textiles and paper. Also serves as a building block in the development of pharmaceuticals, particularly in the creation of naphthyl-based derivatives with biological activity. Its structure supports use in organic semiconductors and photochemical materials. Frequently utilized in research for labeling and derivatization in analytical chemistry.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿470.00
inventory 100g
10-20 days ฿1,750.00
inventory 500g
10-20 days ฿8,680.00

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6-Bromo-2-naphthol
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Used as an intermediate in the synthesis of dyes and fluorescent compounds due to its ability to undergo coupling reactions and halogen displacement. Commonly employed in the production of optical brighteners for textiles and paper. Also serves as a building block in the development of pharmaceuticals, particularly in the creation of naphthyl-based derivatives with biological activity. Its structure supports use in organic semiconductors and photochemical materials. Frequently utilized in research for la

Used as an intermediate in the synthesis of dyes and fluorescent compounds due to its ability to undergo coupling reactions and halogen displacement. Commonly employed in the production of optical brighteners for textiles and paper. Also serves as a building block in the development of pharmaceuticals, particularly in the creation of naphthyl-based derivatives with biological activity. Its structure supports use in organic semiconductors and photochemical materials. Frequently utilized in research for labeling and derivatization in analytical chemistry.

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