4-Methoxy-2,3,6-trimethylbenzenesulfonyl Chloride

95%

Reagent Code: #208123
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CAS Number 80745-07-9

science Other reagents with same CAS 80745-07-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.73 g/mol
Formula C₁₀H₁₃ClO₃S
badge Registry Numbers
MDL Number MFCD00038846
thermostat Physical Properties
Melting Point 57-61°C
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used primarily as a sulfonylating agent in organic synthesis, this compound is especially valuable in the preparation of sulfonate esters and sulfonamides, which are key intermediates in pharmaceuticals and agrochemicals. Its electron-rich aromatic ring enhances reactivity and selectivity in coupling reactions. It is also employed in the development of photoacid generators for advanced lithography in semiconductor manufacturing. Due to the presence of methoxy and methyl groups, it offers improved solubility and stability in common organic solvents, making it suitable for use in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,670.00
4-Methoxy-2,3,6-trimethylbenzenesulfonyl Chloride
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Used primarily as a sulfonylating agent in organic synthesis, this compound is especially valuable in the preparation of sulfonate esters and sulfonamides, which are key intermediates in pharmaceuticals and agrochemicals. Its electron-rich aromatic ring enhances reactivity and selectivity in coupling reactions. It is also employed in the development of photoacid generators for advanced lithography in semiconductor manufacturing. Due to the presence of methoxy and methyl groups, it offers improved solubil

Used primarily as a sulfonylating agent in organic synthesis, this compound is especially valuable in the preparation of sulfonate esters and sulfonamides, which are key intermediates in pharmaceuticals and agrochemicals. Its electron-rich aromatic ring enhances reactivity and selectivity in coupling reactions. It is also employed in the development of photoacid generators for advanced lithography in semiconductor manufacturing. Due to the presence of methoxy and methyl groups, it offers improved solubility and stability in common organic solvents, making it suitable for use in multi-step synthetic routes.

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