3-Bromo-4-Methoxybenzenesulfonyl Chloride

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Reagent Code: #147141
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CAS Number 23094-96-4

science Other reagents with same CAS 23094-96-4

blur_circular Chemical Specifications

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Weight 285.54 g/mol
Formula C₇H₆BrClO₃S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It participates in the preparation of sulfonamide derivatives, which are key structures in various bioactive molecules and drug candidates. Its reactivity allows for the introduction of sulfonyl groups into aromatic systems, facilitating the development of compounds with antimicrobial, anti-inflammatory, or kinase-inhibiting properties. Commonly employed in cross-coupling reactions and electrophilic substitutions due to the presence of both bromo and sulfonyl chloride functional groups, enabling selective modifications in complex molecule assembly. Also utilized in agrochemical synthesis for building functionalized aromatic frameworks.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿599.50
inventory 5g
10-20 days ฿2,244.00

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3-Bromo-4-Methoxybenzenesulfonyl Chloride
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It participates in the preparation of sulfonamide derivatives, which are key structures in various bioactive molecules and drug candidates. Its reactivity allows for the introduction of sulfonyl groups into aromatic systems, facilitating the development of compounds with antimicrobial, anti-inflammatory, or kinase-inhibiting properties. Commonly employed in cross-coupling reactions and electrophilic substit

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry. It participates in the preparation of sulfonamide derivatives, which are key structures in various bioactive molecules and drug candidates. Its reactivity allows for the introduction of sulfonyl groups into aromatic systems, facilitating the development of compounds with antimicrobial, anti-inflammatory, or kinase-inhibiting properties. Commonly employed in cross-coupling reactions and electrophilic substitutions due to the presence of both bromo and sulfonyl chloride functional groups, enabling selective modifications in complex molecule assembly. Also utilized in agrochemical synthesis for building functionalized aromatic frameworks.

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