6-Bromoisothiazolo[4,3-b]pyridine

95%

Reagent Code: #142249
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CAS Number 2222541-50-4

science Other reagents with same CAS 2222541-50-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.07 g/mol
Formula C₆H₃BrN₂S
thermostat Physical Properties
Boiling Point 278.1±20.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.859±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of kinase inhibitors and antimicrobial agents due to its isothiazole core, which enhances binding affinity to enzyme active sites. Its bromine functionality allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿12,980.00
50mg
10-20 days ฿22,060.00
100mg
10-20 days ฿37,490.00
6-Bromoisothiazolo[4,3-b]pyridine
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of kinase inhibitors and antimicrobial agents due to its isothiazole core, which enhances binding affinity to enzyme active sites. Its bromine functionality allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship stud

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block in the development of kinase inhibitors and antimicrobial agents due to its isothiazole core, which enhances binding affinity to enzyme active sites. Its bromine functionality allows for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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