Methyl3-bromo-5-(chlorosulfonyl)benzoate

98%

Reagent Code: #213567
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CAS Number 668261-21-0

science Other reagents with same CAS 668261-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.55 g/mol
Formula C₈H₆BrClO₄S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl and bromo groups allow for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in the preparation of sulfonamide derivatives, which are key structural motifs in various bioactive compounds, including antimicrobial and anti-inflammatory agents. Also utilized in the development of crop protection chemicals due to its ability to introduce specific substituents into aromatic systems. Its ester group facilitates further transformation, enabling its use in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,280.00
inventory 250mg
10-20 days ฿7,150.00
inventory 1g
10-20 days ฿14,310.00
inventory 5g
10-20 days ฿47,210.00
Methyl3-bromo-5-(chlorosulfonyl)benzoate
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl and bromo groups allow for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in the preparation of sulfonamide derivatives, which are key structural motifs in various bioactive compounds, including antimicrobial and anti-inflammatory agents. Also utilized in the development of crop protection chemicals due to its ability to introduce s

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive chlorosulfonyl and bromo groups allow for selective functionalization, making it valuable in building complex organic molecules. Commonly employed in the preparation of sulfonamide derivatives, which are key structural motifs in various bioactive compounds, including antimicrobial and anti-inflammatory agents. Also utilized in the development of crop protection chemicals due to its ability to introduce specific substituents into aromatic systems. Its ester group facilitates further transformation, enabling its use in multi-step synthetic routes.

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