2-Bromo-5-methoxyaniline

98%

Reagent Code: #151576
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CAS Number 59557-92-5

science Other reagents with same CAS 59557-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.05 g/mol
Formula C₇H₈BrNO
badge Registry Numbers
MDL Number MFCD00070741
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of dyes and pigments. It serves as a building block in the production of certain triarylmethane dyes and functionalized aniline derivatives. Its bromo and methoxy groups allow for selective cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry for creating complex aromatic structures. Also employed in the preparation of photochromic and electroactive materials.

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Test Parameter Specification
Appearance Brown to black solid-liquid mixture
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿480.00
inventory 25g
10-20 days ฿2,280.00
inventory 100g
10-20 days ฿8,760.00

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2-Bromo-5-methoxyaniline
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of dyes and pigments. It serves as a building block in the production of certain triarylmethane dyes and functionalized aniline derivatives. Its bromo and methoxy groups allow for selective cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry for creating complex aromatic structures. Also employed in the preparation of photochromic and electroactive materials

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of dyes and pigments. It serves as a building block in the production of certain triarylmethane dyes and functionalized aniline derivatives. Its bromo and methoxy groups allow for selective cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry for creating complex aromatic structures. Also employed in the preparation of photochromic and electroactive materials.

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