N-(2-nitrophenyl)formamide

≥95%

Reagent Code: #216058
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CAS Number 7418-32-8

science Other reagents with same CAS 7418-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.13 g/mol
Formula C₇H₆N₂O₃
badge Registry Numbers
MDL Number MFCD00088780
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and dyes. It serves as a building block in the development of pharmaceuticals, where the nitrophenyl group can be reduced to an aminophenyl derivative for further functionalization. Also employed in photochemistry due to the light-sensitive nature of the o-nitro group, making it useful in photolabile protecting group strategies. Its structure allows for participation in cyclization reactions, contributing to the synthesis of benzimidazoles and related nitrogen-containing rings.

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inventory 1g
10-20 days ฿39,780.00

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N-(2-nitrophenyl)formamide
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Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and dyes. It serves as a building block in the development of pharmaceuticals, where the nitrophenyl group can be reduced to an aminophenyl derivative for further functionalization. Also employed in photochemistry due to the light-sensitive nature of the o-nitro group, making it useful in photolabile protecting group strategies. Its structure allows for participation in cyclization reactions, contributing
Used as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and dyes. It serves as a building block in the development of pharmaceuticals, where the nitrophenyl group can be reduced to an aminophenyl derivative for further functionalization. Also employed in photochemistry due to the light-sensitive nature of the o-nitro group, making it useful in photolabile protecting group strategies. Its structure allows for participation in cyclization reactions, contributing to the synthesis of benzimidazoles and related nitrogen-containing rings.
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