2-Bromo-6,7-dihydrothiazolo[5,4-c]pyridin-4(5H)-one
≥95%
- Product Code: 116737
CAS:
1035219-96-5
Molecular Weight: | 233.09 g./mol | Molecular Formula: | C₆H₅BrN₂OS |
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EC Number: | MDL Number: | MFCD14706758 | |
Melting Point: | Boiling Point: | 487.7°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a bromine atom and a fused thiazolopyridine ring system, makes it a valuable building block for developing potential drug candidates. Researchers often employ it in the design and synthesis of compounds targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, anticancer, and antimicrobial agents. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for high-throughput screening in drug discovery programs.
Product Specification:
Test | Specification |
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Appearance | Solid |
Purity (%) | 94.5-100 |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿5,175.00 |
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0.250 | 10-20 days | ฿9,270.00 |
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1.000 | 10-20 days | ฿25,182.00 |
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2-Bromo-6,7-dihydrothiazolo[5,4-c]pyridin-4(5H)-one
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a bromine atom and a fused thiazolopyridine ring system, makes it a valuable building block for developing potential drug candidates. Researchers often employ it in the design and synthesis of compounds targeting specific enzymes or receptors, particularly in the development of anti-inflammatory, anticancer, and antimicrobial agents. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for high-throughput screening in drug discovery programs.
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