2-Chloro-5-nitrobenzamide

95%

Reagent Code: #131173
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CAS Number 16588-15-1

science Other reagents with same CAS 16588-15-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.58 g/mol
Formula C₇H₅ClN₂O₃
badge Registry Numbers
MDL Number MFCD00088420
thermostat Physical Properties
Melting Point 178 °C
Boiling Point 299.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.520±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of certain herbicides and plant growth regulators due to its ability to modify biological activity in targeted compounds. Its nitro and amide functional groups make it valuable in organic synthesis for building more complex molecules. Also utilized in research settings for developing new bioactive compounds, especially those involving chlorinated aromatic scaffolds.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿17,170.00
inventory 5g
10-20 days ฿4,910.00

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2-Chloro-5-nitrobenzamide
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of certain herbicides and plant growth regulators due to its ability to modify biological activity in targeted compounds. Its nitro and amide functional groups make it valuable in organic synthesis for building more complex molecules. Also utilized in research settings for developing new bioactive compounds, especially those involving chlorinated aromatic scaffolds.

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It plays a key role in the production of certain herbicides and plant growth regulators due to its ability to modify biological activity in targeted compounds. Its nitro and amide functional groups make it valuable in organic synthesis for building more complex molecules. Also utilized in research settings for developing new bioactive compounds, especially those involving chlorinated aromatic scaffolds.

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