3,4-Difluorobenzenesulfonylchloride

98%

Reagent Code: #170271
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CAS Number 145758-05-0

science Other reagents with same CAS 145758-05-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.60 g/mol
Formula C₆H₃ClF₂O₂S
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamides and sulfonate esters—common motifs in drug design. It is especially useful in the development of bioactive molecules where the difluorobenzene moiety enhances metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electronic and steric influence of the fluorine atoms. Also utilized in the preparation of functionalized polymers and specialty materials requiring thermal and chemical resistance.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿162.00
5g
10-20 days ฿310.00
100g
10-20 days ฿5,690.00
25g
10-20 days ฿1,530.00

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3,4-Difluorobenzenesulfonylchloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamides and sulfonate esters—common motifs in drug design. It is especially useful in the development of bioactive molecules where the difluorobenzene moiety enhances metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due t

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing sulfonamides and sulfonate esters—common motifs in drug design. It is especially useful in the development of bioactive molecules where the difluorobenzene moiety enhances metabolic stability and membrane permeability. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electronic and steric influence of the fluorine atoms. Also utilized in the preparation of functionalized polymers and specialty materials requiring thermal and chemical resistance.

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