m-Toluenesulfonyl chloride

≥97 %

Reagent Code: #240619
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CAS Number 1899-93-0

science Other reagents with same CAS 1899-93-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.65 g/mol
Formula C₇H₇ClO₂S
badge Registry Numbers
MDL Number MFCD00051747
thermostat Physical Properties
Boiling Point 252-253°C (Lit.)
inventory_2 Storage & Handling
Density 1.3140 g/cm3
Storage Room temperature, dry

description Product Description

Used primarily as a reagent in organic synthesis, particularly for introducing the sulfonyl group into molecules. It is commonly employed to convert alcohols into sulfonate esters, which are good leaving groups in nucleophilic substitution reactions. Widely used in the preparation of pharmaceuticals, agrochemicals, and dyes due to its ability to modify functional groups and enhance reaction pathways. Also serves as a protecting group agent for amines and alcohols in multi-step syntheses. Its reactivity makes it valuable in peptide synthesis and in the production of sulfonamide-based compounds, which are key in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿590.00
inventory 5g
10-20 days ฿1,550.00
inventory 25g
10-20 days ฿6,120.00

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m-Toluenesulfonyl chloride
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Used primarily as a reagent in organic synthesis, particularly for introducing the sulfonyl group into molecules. It is commonly employed to convert alcohols into sulfonate esters, which are good leaving groups in nucleophilic substitution reactions. Widely used in the preparation of pharmaceuticals, agrochemicals, and dyes due to its ability to modify functional groups and enhance reaction pathways. Also serves as a protecting group agent for amines and alcohols in multi-step syntheses. Its reactivity m

Used primarily as a reagent in organic synthesis, particularly for introducing the sulfonyl group into molecules. It is commonly employed to convert alcohols into sulfonate esters, which are good leaving groups in nucleophilic substitution reactions. Widely used in the preparation of pharmaceuticals, agrochemicals, and dyes due to its ability to modify functional groups and enhance reaction pathways. Also serves as a protecting group agent for amines and alcohols in multi-step syntheses. Its reactivity makes it valuable in peptide synthesis and in the production of sulfonamide-based compounds, which are key in medicinal chemistry.

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