3,4-Dichlorobenzenemethanesulfonamide

98%

Reagent Code: #180125
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CAS Number 904674-08-4

science Other reagents with same CAS 904674-08-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.11 g/mol
Formula C₇H₇Cl₂NO₂S
badge Registry Numbers
MDL Number MFCD11205043
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of diuretic agents and other bioactive molecules. Its sulfonamide group enables it to participate in reactions that form carbon-sulfur or carbon-nitrogen bonds, making it valuable in medicinal chemistry. It is also employed in the preparation of agrochemicals and functionalized aromatic compounds where chlorinated aromatic rings enhance reactivity or stability. Its structure allows for selective derivatization, supporting research in drug design and optimization.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿18,200.00
inventory 5g
10-20 days ฿67,060.00

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3,4-Dichlorobenzenemethanesulfonamide
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of diuretic agents and other bioactive molecules. Its sulfonamide group enables it to participate in reactions that form carbon-sulfur or carbon-nitrogen bonds, making it valuable in medicinal chemistry. It is also employed in the preparation of agrochemicals and functionalized aromatic compounds where chlorinated aromatic rings enhance reactivity or stability. Its structure allows for selective derivatization, s

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of diuretic agents and other bioactive molecules. Its sulfonamide group enables it to participate in reactions that form carbon-sulfur or carbon-nitrogen bonds, making it valuable in medicinal chemistry. It is also employed in the preparation of agrochemicals and functionalized aromatic compounds where chlorinated aromatic rings enhance reactivity or stability. Its structure allows for selective derivatization, supporting research in drug design and optimization.

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