1-Propanesulfonyl chloride

98%

Reagent Code: #224998
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Alias Propylsulfonyl chloride
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CAS Number 10147-36-1

science Other reagents with same CAS 10147-36-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.60 g/mol
Formula C₃H₇ClO₂S
badge Registry Numbers
MDL Number MFCD00007462
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as a sulfonating agent in organic synthesis, enabling the introduction of propanesulfonyl groups into various compounds. Commonly applied in the pharmaceutical industry for modifying drug molecules to improve stability and bioavailability. Also utilized in the preparation of agrochemicals and dyes, where sulfonyl chloride functionality enhances reactivity or structural properties. Its role in peptide chemistry includes protecting group manipulation and activation of carboxylic acids. Handles under anhydrous conditions due to high reactivity with moisture.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿420.00
100g
10-20 days ฿1,250.00
500g
10-20 days ฿6,020.00
2.5kg
10-20 days ฿29,740.00
1-Propanesulfonyl chloride
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Used primarily as a sulfonating agent in organic synthesis, enabling the introduction of propanesulfonyl groups into various compounds. Commonly applied in the pharmaceutical industry for modifying drug molecules to improve stability and bioavailability. Also utilized in the preparation of agrochemicals and dyes, where sulfonyl chloride functionality enhances reactivity or structural properties. Its role in peptide chemistry includes protecting group manipulation and activation of carboxylic acids. Handl

Used primarily as a sulfonating agent in organic synthesis, enabling the introduction of propanesulfonyl groups into various compounds. Commonly applied in the pharmaceutical industry for modifying drug molecules to improve stability and bioavailability. Also utilized in the preparation of agrochemicals and dyes, where sulfonyl chloride functionality enhances reactivity or structural properties. Its role in peptide chemistry includes protecting group manipulation and activation of carboxylic acids. Handles under anhydrous conditions due to high reactivity with moisture.

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