2-(2-Bromo-pyridin-3-yloxy)-benzothiazole

97%

Reagent Code: #152205
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CAS Number 1065484-73-2

science Other reagents with same CAS 1065484-73-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.166 g/mol
Formula C₁₂H₇BrN₂OS
badge Registry Numbers
MDL Number MFCD10698951
inventory_2 Storage & Handling
Density 1.649 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of antitumor agents and anti-inflammatory drugs. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its bromo functional group allows for further cross-coupling reactions, making it valuable in structure-activity relationship studies.

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inventory 500mg
10-20 days ฿39,720.00

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2-(2-Bromo-pyridin-3-yloxy)-benzothiazole
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of antitumor agents and anti-inflammatory drugs. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its bromo functional
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form stable heterocyclic structures that interact with biological targets. Commonly employed in the preparation of antitumor agents and anti-inflammatory drugs. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and efficacy. Its bromo functional group allows for further cross-coupling reactions, making it valuable in structure-activity relationship studies.
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