4-Amino-6-bromothiochroman 1,1-dioxide hydrochloride
97%
- Product Code: 119043
CAS:
1172986-17-2
Molecular Weight: | 312.61 g./mol | Molecular Formula: | C₉H₁₁BrClNO₂S |
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EC Number: | MDL Number: | MFCD11616744 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a thiochroman core with amino and bromo substituents, makes it a valuable intermediate in the creation of molecules with potential therapeutic properties. It is often explored in the design of compounds targeting neurological disorders, as the thiochroman scaffold is known to interact with central nervous system receptors. Additionally, its bromo group allows for further functionalization, enabling the development of diverse chemical libraries for high-throughput screening in drug discovery. Researchers also investigate its potential in the synthesis of anti-inflammatory or anticancer agents, leveraging its unique chemical reactivity and structural features.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿4,464.00 |
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0.250 | 10-20 days | ฿7,119.00 |
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1.000 | 10-20 days | ฿18,180.00 |
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5.000 | 10-20 days | ฿55,656.00 |
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4-Amino-6-bromothiochroman 1,1-dioxide hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a thiochroman core with amino and bromo substituents, makes it a valuable intermediate in the creation of molecules with potential therapeutic properties. It is often explored in the design of compounds targeting neurological disorders, as the thiochroman scaffold is known to interact with central nervous system receptors. Additionally, its bromo group allows for further functionalization, enabling the development of diverse chemical libraries for high-throughput screening in drug discovery. Researchers also investigate its potential in the synthesis of anti-inflammatory or anticancer agents, leveraging its unique chemical reactivity and structural features.
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