Methyl 2-(Chlorosulfonyl)acetate

≥95%

Reagent Code: #173654
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CAS Number 56146-83-9

science Other reagents with same CAS 56146-83-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.59 g/mol
Formula C₃H₅ClO₄S
badge Registry Numbers
MDL Number MFCD00075558
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key reagent in the preparation of sulfonamide derivatives, which are important structural motifs in many biologically active compounds. Its reactivity allows for the introduction of sulfonyl groups into target molecules, facilitating the development of drugs with antimicrobial, anti-inflammatory, or antidiabetic properties. Additionally, it is employed in the synthesis of functionalized esters and heterocyclic compounds. Due to its high reactivity and sensitivity to moisture, it is handled under controlled conditions, typically in anhydrous environments.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,480.00
inventory 10g
10-20 days ฿16,000.00
inventory 25g
10-20 days ฿36,800.00
inventory 1g
10-20 days ฿1,920.00

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Methyl 2-(Chlorosulfonyl)acetate
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key reagent in the preparation of sulfonamide derivatives, which are important structural motifs in many biologically active compounds. Its reactivity allows for the introduction of sulfonyl groups into target molecules, facilitating the development of drugs with antimicrobial, anti-inflammatory, or antidiabetic properties. Additionally, it is employed in the synthesis of

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. It serves as a key reagent in the preparation of sulfonamide derivatives, which are important structural motifs in many biologically active compounds. Its reactivity allows for the introduction of sulfonyl groups into target molecules, facilitating the development of drugs with antimicrobial, anti-inflammatory, or antidiabetic properties. Additionally, it is employed in the synthesis of functionalized esters and heterocyclic compounds. Due to its high reactivity and sensitivity to moisture, it is handled under controlled conditions, typically in anhydrous environments.

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