(2-Amino-3-nitrophenyl)methanol

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Reagent Code: #137558
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CAS Number 139743-08-1

science Other reagents with same CAS 139743-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.15 g/mol
Formula C₇H₈N₂O₃
badge Registry Numbers
MDL Number MFCD09880172
inventory_2 Storage & Handling
Storage 2-8°C, away from light, dry, sealed

description Product Description

Used as an intermediate in the synthesis of dyes and pigments, particularly for producing azo dyes that exhibit good light and wash fastness. It also serves in the preparation of pharmaceuticals, where the amino and hydroxyl functional groups allow for derivatization into active drug compounds. Additionally, it finds use in the development of agrochemicals, contributing to the creation of certain herbicides and plant growth regulators. Its nitro group can be reduced to an amine, enabling further chemical transformations in multi-step organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿840.00
inventory 1g
10-20 days ฿3,110.00
inventory 5g
10-20 days ฿15,460.00
inventory 10g
10-20 days ฿30,880.00
inventory 25g
10-20 days ฿67,100.00

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(2-Amino-3-nitrophenyl)methanol
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Used as an intermediate in the synthesis of dyes and pigments, particularly for producing azo dyes that exhibit good light and wash fastness. It also serves in the preparation of pharmaceuticals, where the amino and hydroxyl functional groups allow for derivatization into active drug compounds. Additionally, it finds use in the development of agrochemicals, contributing to the creation of certain herbicides and plant growth regulators. Its nitro group can be reduced to an amine, enabling further chemical

Used as an intermediate in the synthesis of dyes and pigments, particularly for producing azo dyes that exhibit good light and wash fastness. It also serves in the preparation of pharmaceuticals, where the amino and hydroxyl functional groups allow for derivatization into active drug compounds. Additionally, it finds use in the development of agrochemicals, contributing to the creation of certain herbicides and plant growth regulators. Its nitro group can be reduced to an amine, enabling further chemical transformations in multi-step organic syntheses.

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