1-bromo-2-methyl-4-nitronaphthalene

95%

Reagent Code: #150434
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CAS Number 10317-70-1

science Other reagents with same CAS 10317-70-1

blur_circular Chemical Specifications

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Weight 266.09 g/mol
Formula C₁₁H₈BrNO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly for producing vat dyes and disperse dyes that exhibit good lightfastness and color strength. It also serves in the preparation of functionalized naphthalene derivatives for use in agrochemicals and pharmaceuticals. Its nitro and bromo groups allow for selective substitution reactions, making it valuable in organic synthesis for constructing complex aromatic systems. Additionally, it has been explored in the development of organic semiconductors and fluorescent probes due to its extended aromatic structure and electron-withdrawing properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,260.00
inventory 250mg
10-20 days ฿2,530.00
inventory 1g
10-20 days ฿7,580.00

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1-bromo-2-methyl-4-nitronaphthalene
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Used as an intermediate in the synthesis of dyes and pigments, particularly for producing vat dyes and disperse dyes that exhibit good lightfastness and color strength. It also serves in the preparation of functionalized naphthalene derivatives for use in agrochemicals and pharmaceuticals. Its nitro and bromo groups allow for selective substitution reactions, making it valuable in organic synthesis for constructing complex aromatic systems. Additionally, it has been explored in the development of organic

Used as an intermediate in the synthesis of dyes and pigments, particularly for producing vat dyes and disperse dyes that exhibit good lightfastness and color strength. It also serves in the preparation of functionalized naphthalene derivatives for use in agrochemicals and pharmaceuticals. Its nitro and bromo groups allow for selective substitution reactions, making it valuable in organic synthesis for constructing complex aromatic systems. Additionally, it has been explored in the development of organic semiconductors and fluorescent probes due to its extended aromatic structure and electron-withdrawing properties.

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