alpha-Toluenesulfonyl chloride

98%

Reagent Code: #240368
label
Alias α-toluenesulfonyl chloride; benzylsulfonyl chloride; benzylmethylsulfonyl chloride
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CAS Number 1939-99-7

science Other reagents with same CAS 1939-99-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.64 g/mol
Formula C₇H₇ClO₂S
badge Registry Numbers
MDL Number MFCD00007455
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as a reagent in organic synthesis, it serves to introduce the tosyl group, which acts as a protecting group for alcohols and amines. It is widely employed in the preparation of sulfonate esters and sulfonamides, important intermediates in pharmaceutical manufacturing. Its reactivity makes it valuable in the activation of hydroxyl groups for nucleophilic substitution reactions. Commonly used in the production of dyes, agrochemicals, and certain active pharmaceutical ingredients where controlled functional group transformation is required.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿720.00
inventory 100g
10-20 days ฿2,450.00
inventory 500g
10-20 days ฿9,990.00
alpha-Toluenesulfonyl chloride
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Used primarily as a reagent in organic synthesis, it serves to introduce the tosyl group, which acts as a protecting group for alcohols and amines. It is widely employed in the preparation of sulfonate esters and sulfonamides, important intermediates in pharmaceutical manufacturing. Its reactivity makes it valuable in the activation of hydroxyl groups for nucleophilic substitution reactions. Commonly used in the production of dyes, agrochemicals, and certain active pharmaceutical ingredients where contro

Used primarily as a reagent in organic synthesis, it serves to introduce the tosyl group, which acts as a protecting group for alcohols and amines. It is widely employed in the preparation of sulfonate esters and sulfonamides, important intermediates in pharmaceutical manufacturing. Its reactivity makes it valuable in the activation of hydroxyl groups for nucleophilic substitution reactions. Commonly used in the production of dyes, agrochemicals, and certain active pharmaceutical ingredients where controlled functional group transformation is required.

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