methyl 3-chloro-2-(chlorosulfonyl)benzoate

≥95%

Reagent Code: #203786
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CAS Number 99943-42-7

science Other reagents with same CAS 99943-42-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.1018 g/mol
Formula C₈H₆Cl₂O₄S
badge Registry Numbers
MDL Number MFCD28383771
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 sulfonyl chloride and ester groups allow for sequential functionalization, making it valuable in constructing 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 herbicides and plant growth regulators due to its ability to modify aromatic scaffolds with chlorine and sulfonyl functionalities. Its versatility in cross-coupling and substitution reactions enhances its utility in medicinal chemistry and crop protection research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,400.00
inventory 1g
10-20 days ฿43,200.00

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methyl 3-chloro-2-(chlorosulfonyl)benzoate
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sulfonyl chloride and ester groups allow for sequential functionalization, making it valuable in constructing 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 herbicides and plant growth regulators due to its a

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive sulfonyl chloride and ester groups allow for sequential functionalization, making it valuable in constructing 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 herbicides and plant growth regulators due to its ability to modify aromatic scaffolds with chlorine and sulfonyl functionalities. Its versatility in cross-coupling and substitution reactions enhances its utility in medicinal chemistry and crop protection research.

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