2,5-Dichloro-4-methoxyaniline

95%

Reagent Code: #177507
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CAS Number 101251-23-4

science Other reagents with same CAS 101251-23-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.04 g/mol
Formula C₇H₇Cl₂NO
badge Registry Numbers
MDL Number MFCD16606083
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of dyes and pigments, especially in the production of azo dyes which are valued for their color fastness and wide range of hues. It also serves in the manufacture of certain agricultural chemicals, including herbicides and fungicides, due to its ability to act as a building block in more complex molecules. Additionally, it finds use in the development of specialty polymers and pharmaceuticals where chlorinated aniline derivatives enhance stability and bioactivity. Its methoxy and chloro functional groups allow for selective reactions, making it valuable in fine chemical synthesis.

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Test Parameter Specification
Appearance Solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,020.00
inventory 5g
10-20 days ฿5,750.00
inventory 25g
10-20 days ฿22,880.00

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2,5-Dichloro-4-methoxyaniline
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Used primarily as an intermediate in the synthesis of dyes and pigments, especially in the production of azo dyes which are valued for their color fastness and wide range of hues. It also serves in the manufacture of certain agricultural chemicals, including herbicides and fungicides, due to its ability to act as a building block in more complex molecules. Additionally, it finds use in the development of specialty polymers and pharmaceuticals where chlorinated aniline derivatives enhance stability and bi

Used primarily as an intermediate in the synthesis of dyes and pigments, especially in the production of azo dyes which are valued for their color fastness and wide range of hues. It also serves in the manufacture of certain agricultural chemicals, including herbicides and fungicides, due to its ability to act as a building block in more complex molecules. Additionally, it finds use in the development of specialty polymers and pharmaceuticals where chlorinated aniline derivatives enhance stability and bioactivity. Its methoxy and chloro functional groups allow for selective reactions, making it valuable in fine chemical synthesis.

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