Methyl 2-(chlorosulfonyl)benzoate

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Reagent Code: #206720
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CAS Number 26638-43-7

science Other reagents with same CAS 26638-43-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.66 g/mol
Formula C₈H₇ClO₄S
badge Registry Numbers
MDL Number MFCD00009797
thermostat Physical Properties
Melting Point 62-63°C
Boiling Point 344.8°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for constructing sulfonamide-based drugs. It reacts with amines to form sulfonamides, which are key structural motifs in many bioactive molecules, including antibiotics and anti-inflammatory agents. Also employed in the preparation of dyes and agrochemicals due to its ability to introduce sulfonyl functional groups. Its reactivity makes it valuable in the development of specialty chemicals requiring selective sulfonylation.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿180.00
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿1,150.00
inventory 25g
10-20 days ฿5,620.00
inventory 100g
10-20 days ฿22,420.00

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Methyl 2-(chlorosulfonyl)benzoate
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Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for constructing sulfonamide-based drugs. It reacts with amines to form sulfonamides, which are key structural motifs in many bioactive molecules, including antibiotics and anti-inflammatory agents. Also employed in the preparation of dyes and agrochemicals due to its ability to introduce sulfonyl functional groups. Its reactivity makes it valuable in the development of specialty chemicals requiring selective s
Used primarily as an intermediate in organic synthesis, especially in the pharmaceutical industry for constructing sulfonamide-based drugs. It reacts with amines to form sulfonamides, which are key structural motifs in many bioactive molecules, including antibiotics and anti-inflammatory agents. Also employed in the preparation of dyes and agrochemicals due to its ability to introduce sulfonyl functional groups. Its reactivity makes it valuable in the development of specialty chemicals requiring selective sulfonylation.
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