2-Methyl-1H-imidazole-5-sulfonyl chloride

≥95%

Reagent Code: #203509
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CAS Number 205311-54-2

science Other reagents with same CAS 205311-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.61 g/mol
Formula C₄H₅ClN₂O₂S
badge Registry Numbers
MDL Number MFCD19596983
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of sulfa drugs, particularly in the preparation of sulfonamide antibiotics. It plays an important role in medicinal chemistry for constructing biologically active molecules by introducing the sulfonyl chloride functional group to nitrogen-containing heterocycles. Its reactivity allows for efficient coupling with amines to form sulfonamides, which are essential structural motifs in antimicrobial and anti-inflammatory agents. Also utilized in the development of agrochemicals and functional materials due to its ability to modify molecular properties through sulfonylation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,210.00
inventory 250mg
10-20 days ฿11,120.00
inventory 1g
10-20 days ฿33,480.00
2-Methyl-1H-imidazole-5-sulfonyl chloride
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Used as a key intermediate in the synthesis of sulfa drugs, particularly in the preparation of sulfonamide antibiotics. It plays an important role in medicinal chemistry for constructing biologically active molecules by introducing the sulfonyl chloride functional group to nitrogen-containing heterocycles. Its reactivity allows for efficient coupling with amines to form sulfonamides, which are essential structural motifs in antimicrobial and anti-inflammatory agents. Also utilized in the development of a

Used as a key intermediate in the synthesis of sulfa drugs, particularly in the preparation of sulfonamide antibiotics. It plays an important role in medicinal chemistry for constructing biologically active molecules by introducing the sulfonyl chloride functional group to nitrogen-containing heterocycles. Its reactivity allows for efficient coupling with amines to form sulfonamides, which are essential structural motifs in antimicrobial and anti-inflammatory agents. Also utilized in the development of agrochemicals and functional materials due to its ability to modify molecular properties through sulfonylation.

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