Methyl3-(Chlorosulfonyl)benzoate

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Reagent Code: #205817
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CAS Number 63555-50-0

science Other reagents with same CAS 63555-50-0

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Weight 234.66 g/mol
Formula C₈H₇ClO₄S
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MDL Number MFCD06408800
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Storage Room temperature

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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the preparation of sulfonamide-based drugs. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many medicinal compounds, including antibiotics and anti-inflammatory agents. Also employed in the development of agrochemicals and dyes due to its ability to introduce sulfonyl functionalities into aromatic systems. The ester group allows for further derivatization, making it a versatile building block in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,910.00
inventory 10g
10-20 days ฿3,800.00
inventory 25g
10-20 days ฿8,790.00

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Methyl3-(Chlorosulfonyl)benzoate
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the preparation of sulfonamide-based drugs. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many medicinal compounds, including antibiotics and anti-inflammatory agents. Also employed in the development of agrochemicals and dyes due to its ability to introduce sulfonyl functionalities into aromatic systems. The ester group allows for furth

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the preparation of sulfonamide-based drugs. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many medicinal compounds, including antibiotics and anti-inflammatory agents. Also employed in the development of agrochemicals and dyes due to its ability to introduce sulfonyl functionalities into aromatic systems. The ester group allows for further derivatization, making it a versatile building block in multi-step syntheses.

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