4-Nitrobenzenediazonium Tetrafluoroborate

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Reagent Code: #91152
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CAS Number 456-27-9

science Other reagents with same CAS 456-27-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.92 g/mol
Formula C₆H₄BF₄N₃O₂
badge Registry Numbers
MDL Number MFCD00012005
inventory_2 Storage & Handling
Storage -20°C, inert gas storage

description Product Description

This chemical is primarily used in organic synthesis as a diazonium salt, which is highly reactive and serves as a key intermediate in various chemical reactions. It is commonly employed in the preparation of azo dyes, where it acts as a coupling agent to produce vibrant and stable colorants for textiles, inks, and pigments. Additionally, it is utilized in the synthesis of aryl compounds through Sandmeyer reactions, enabling the replacement of the diazonium group with halogens, cyano groups, or other substituents in nitroaromatic systems. Its role in photoaffinity labeling is also notable, as it helps in studying molecular interactions and binding sites in biochemical research. Due to its reactivity, it is often handled with care in controlled environments.

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Test Parameter Specification
Appearance Pale yellow to brown solid
Purity 96.5
Melting Point 140-150

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,390.00
inventory 25g
10-20 days ฿11,680.00
inventory 1g
10-20 days ฿1,180.00
inventory 100g
10-20 days ฿45,500.00

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4-Nitrobenzenediazonium Tetrafluoroborate
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This chemical is primarily used in organic synthesis as a diazonium salt, which is highly reactive and serves as a key intermediate in various chemical reactions. It is commonly employed in the preparation of azo dyes, where it acts as a coupling agent to produce vibrant and stable colorants for textiles, inks, and pigments. Additionally, it is utilized in the synthesis of aryl compounds through Sandmeyer reactions, enabling the replacement of the diazonium group with halogens, cyano groups, or other sub

This chemical is primarily used in organic synthesis as a diazonium salt, which is highly reactive and serves as a key intermediate in various chemical reactions. It is commonly employed in the preparation of azo dyes, where it acts as a coupling agent to produce vibrant and stable colorants for textiles, inks, and pigments. Additionally, it is utilized in the synthesis of aryl compounds through Sandmeyer reactions, enabling the replacement of the diazonium group with halogens, cyano groups, or other substituents in nitroaromatic systems. Its role in photoaffinity labeling is also notable, as it helps in studying molecular interactions and binding sites in biochemical research. Due to its reactivity, it is often handled with care in controlled environments.

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