2-methylbenzenesulfonyl chloride

75% (contains ca. 23% isomer)

Reagent Code: #205916
label
Alias 2-Toluenesulfonyl chloride
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CAS Number 133-59-5

science Other reagents with same CAS 133-59-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.64 g/mol
Formula C₇H₇ClO₂S
badge Registry Numbers
MDL Number MFCD00024874
thermostat Physical Properties
Boiling Point 254°C(lit.)
inventory_2 Storage & Handling
Density 1.320 g/mL at 25°C(lit.)
Storage Room temperature, sealed

description Product Description

Used primarily as a sulfonating agent in organic synthesis, this compound plays a key role in the preparation of sulfonamides, which are important in pharmaceuticals and agrochemicals. It reacts with amines to form sulfonamide derivatives, a common functional group in drug design, including antibiotics and enzyme inhibitors. It is also employed in the protection of functional groups during multi-step syntheses due to the stability and selective reactivity of the sulfonyl moiety. Additionally, it serves as a reagent in the synthesis of dyes, polymers, and specialty chemicals where controlled sulfonylation is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿950.00
inventory 25g
10-20 days ฿1,710.00
inventory 100g
10-20 days ฿4,620.00
inventory 500g
10-20 days ฿22,560.00

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2-methylbenzenesulfonyl chloride
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Used primarily as a sulfonating agent in organic synthesis, this compound plays a key role in the preparation of sulfonamides, which are important in pharmaceuticals and agrochemicals. It reacts with amines to form sulfonamide derivatives, a common functional group in drug design, including antibiotics and enzyme inhibitors. It is also employed in the protection of functional groups during multi-step syntheses due to the stability and selective reactivity of the sulfonyl moiety. Additionally, it serves a

Used primarily as a sulfonating agent in organic synthesis, this compound plays a key role in the preparation of sulfonamides, which are important in pharmaceuticals and agrochemicals. It reacts with amines to form sulfonamide derivatives, a common functional group in drug design, including antibiotics and enzyme inhibitors. It is also employed in the protection of functional groups during multi-step syntheses due to the stability and selective reactivity of the sulfonyl moiety. Additionally, it serves as a reagent in the synthesis of dyes, polymers, and specialty chemicals where controlled sulfonylation is required.

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