4-Methyl-2-(4-(trifluoromethyl)phenyl)thiazole-5-sulfonyl chloride

98%

Reagent Code: #214411
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CAS Number 568577-83-3

science Other reagents with same CAS 568577-83-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.76 g/mol
Formula C₁₁H₇ClF₃NO₂S₂
badge Registry Numbers
MDL Number MFCD04974054
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its sulfonyl chloride group enables easy attachment to amines or alcohols, facilitating the formation of sulfonamides or sulfonate esters in drug molecules. Also employed in agrochemicals for creating novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl and thiazole moieties. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies targeting inflammatory and oncological pathways.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,800.00
4-Methyl-2-(4-(trifluoromethyl)phenyl)thiazole-5-sulfonyl chloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its sulfonyl chloride group enables easy attachment to amines or alcohols, facilitating the formation of sulfonamides or sulfonate esters in drug molecules. Also employed in agrochemicals for creating novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl and thiazole moieties. Commonly utilized in medicinal chemistry research

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its sulfonyl chloride group enables easy attachment to amines or alcohols, facilitating the formation of sulfonamides or sulfonate esters in drug molecules. Also employed in agrochemicals for creating novel pesticides due to the stability and bioavailability imparted by the trifluoromethyl and thiazole moieties. Commonly utilized in medicinal chemistry research for structure-activity relationship (SAR) studies targeting inflammatory and oncological pathways.

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