4-Chloro-3-nitro-5-sulfamoylbenzoic acid

95%

Reagent Code: #60008
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CAS Number 22892-96-2

science Other reagents with same CAS 22892-96-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.64 g/mol
Formula C₇H₆ClN₂O₆S
badge Registry Numbers
MDL Number MFCD00058688
thermostat Physical Properties
Melting Point 227-231 °C (lit.)
Boiling Point 563.5 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of diuretics and antihypertensive drugs. It plays a key role in the development of compounds that help manage fluid retention and high blood pressure. Additionally, it is utilized in organic chemistry research for creating complex molecules due to its reactive functional groups. Its sulfamoyl and nitro groups make it valuable for further chemical modifications in drug discovery processes.

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Test Parameter Specification
Appearance White to off-white 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 ฿12,033.00

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4-Chloro-3-nitro-5-sulfamoylbenzoic acid
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of diuretics and antihypertensive drugs. It plays a key role in the development of compounds that help manage fluid retention and high blood pressure. Additionally, it is utilized in organic chemistry research for creating complex molecules due to its reactive functional groups. Its sulfamoyl and nitro groups make it valuable for further chemical modifications in drug discovery processes.

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the production of diuretics and antihypertensive drugs. It plays a key role in the development of compounds that help manage fluid retention and high blood pressure. Additionally, it is utilized in organic chemistry research for creating complex molecules due to its reactive functional groups. Its sulfamoyl and nitro groups make it valuable for further chemical modifications in drug discovery processes.

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