3,4-Dichloro-N-(5-chloro-2-(hydrazinylmethyl)phenyl)benzenesulfonamide hydrochloride

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Reagent Code: #179339
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CAS Number 2682114-55-0

science Other reagents with same CAS 2682114-55-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 417.14 g/mol
Formula C₁₃H₁₃Cl₄N₃O₂S
badge Registry Numbers
MDL Number MFCD33022451
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily in research settings as an intermediate for synthesizing biologically active compounds, particularly in the development of potential antimicrobial and antifungal agents. Its hydrazine functionality allows it to participate in condensation reactions, forming hydrazone derivatives that are of interest in medicinal chemistry. It has also been explored in the design of enzyme inhibitors due to the sulfonamide group, which is commonly associated with inhibition of carbonic anhydrase and other metalloenzymes. Due to its reactivity and structural features, it serves as a building block in heterocyclic synthesis, especially for creating fused ring systems with pharmacological potential. Handling requires caution due to the presence of hydrazine, which can be toxic and unstable.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,920.00
inventory 250mg
10-20 days ฿22,860.00
inventory 1g
10-20 days ฿66,840.00
inventory 100mg
10-20 days ฿13,450.00

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3,4-Dichloro-N-(5-chloro-2-(hydrazinylmethyl)phenyl)benzenesulfonamide hydrochloride
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Used primarily in research settings as an intermediate for synthesizing biologically active compounds, particularly in the development of potential antimicrobial and antifungal agents. Its hydrazine functionality allows it to participate in condensation reactions, forming hydrazone derivatives that are of interest in medicinal chemistry. It has also been explored in the design of enzyme inhibitors due to the sulfonamide group, which is commonly associated with inhibition of carbonic anhydrase and other m

Used primarily in research settings as an intermediate for synthesizing biologically active compounds, particularly in the development of potential antimicrobial and antifungal agents. Its hydrazine functionality allows it to participate in condensation reactions, forming hydrazone derivatives that are of interest in medicinal chemistry. It has also been explored in the design of enzyme inhibitors due to the sulfonamide group, which is commonly associated with inhibition of carbonic anhydrase and other metalloenzymes. Due to its reactivity and structural features, it serves as a building block in heterocyclic synthesis, especially for creating fused ring systems with pharmacological potential. Handling requires caution due to the presence of hydrazine, which can be toxic and unstable.

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