3-(2-Bromoacetyl)-5-chlorothiophene-2-sulfonamide

95%

Reagent Code: #44560
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CAS Number 160982-11-6

science Other reagents with same CAS 160982-11-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 318.5958 g/mol
Formula C₆H₅BrClNO₃S₂
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MDL Number MFCD09033310
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Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both bromoacetyl and sulfonamide functional groups, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It is often employed in the preparation of thiophene-based derivatives, which are known for their biological activities, including antimicrobial, anti-inflammatory, and anticancer effects. Additionally, its reactivity allows for further functionalization, enabling researchers to design and synthesize novel compounds for drug discovery and development.

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Test Parameter Specification
Appearance solid or liquid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿2,060.00

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3-(2-Bromoacetyl)-5-chlorothiophene-2-sulfonamide
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This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both bromoacetyl and sulfonamide functional groups, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It is often employed in the preparation of thiophene-based derivatives, which are known for their biological activities, including antimicrobial, anti-inflammatory, and a

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both bromoacetyl and sulfonamide functional groups, makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It is often employed in the preparation of thiophene-based derivatives, which are known for their biological activities, including antimicrobial, anti-inflammatory, and anticancer effects. Additionally, its reactivity allows for further functionalization, enabling researchers to design and synthesize novel compounds for drug discovery and development.

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