PYRIDINE-3-SULFONYL CHLORIDE

98%

Reagent Code: #224887
label
Alias pyrimidine-3-sulfonyl chloride; 3-pyridine-sulfonyl chloride
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CAS Number 16133-25-8

science Other reagents with same CAS 16133-25-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.61 g/mol
Formula C₅H₄ClNO₂S
badge Registry Numbers
MDL Number MFCD04035552
thermostat Physical Properties
Boiling Point 136°C/20mmHg(lit.)
inventory_2 Storage & Handling
Density 1.488
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many biologically active compounds. Commonly employed in the development of herbicides and fungicides due to the stability and polarity imparted by the pyridine ring. Also utilized in research settings for modifying peptides and proteins through selective sulfonamide bond formation. Its aromatic nitrogen enhances solubility and influences the electronic properties of final products, making it valuable in medicinal chemistry for optimizing drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿280.00
5g
10-20 days ฿300.00
25g
10-20 days ฿670.00
100g
10-20 days ฿2,160.00
500g
10-20 days ฿10,140.00
PYRIDINE-3-SULFONYL CHLORIDE
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many biologically active compounds. Commonly employed in the development of herbicides and fungicides due to the stability and polarity imparted by the pyridine ring. Also utilized in research settings for modifying peptides and proteins through selective sulfonamide bond formation. Its aromatic nitrogen en

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines to form sulfonamides, which are key structural motifs in many biologically active compounds. Commonly employed in the development of herbicides and fungicides due to the stability and polarity imparted by the pyridine ring. Also utilized in research settings for modifying peptides and proteins through selective sulfonamide bond formation. Its aromatic nitrogen enhances solubility and influences the electronic properties of final products, making it valuable in medicinal chemistry for optimizing drug candidates.

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