(4,5,6,7-Tetrahydro-1-benzothien-3-ylmethyl)amine hydrochloride
95%
- Product Code: 69081
CAS:
1050509-07-3
| Molecular Weight: | 203.73 g./mol | Molecular Formula: | C₉H₁₄ClNS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09416992 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a tetrahydrobenzothiophene core, makes it a valuable building block for developing compounds with potential therapeutic applications. It is often employed in the design and synthesis of molecules targeting neurological disorders, such as antidepressants or anxiolytics, due to its ability to interact with specific receptors in the brain. Additionally, its amine functionality allows for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Researchers also explore its use in the development of novel drugs for cardiovascular diseases and inflammation, leveraging its unique chemical scaffold to optimize drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,115.00 |
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| 0.250 | 10-20 days | ฿3,582.00 |
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| 1.000 | 10-20 days | ฿9,657.00 |
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(4,5,6,7-Tetrahydro-1-benzothien-3-ylmethyl)amine hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure, featuring a tetrahydrobenzothiophene core, makes it a valuable building block for developing compounds with potential therapeutic applications. It is often employed in the design and synthesis of molecules targeting neurological disorders, such as antidepressants or anxiolytics, due to its ability to interact with specific receptors in the brain. Additionally, its amine functionality allows for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. Researchers also explore its use in the development of novel drugs for cardiovascular diseases and inflammation, leveraging its unique chemical scaffold to optimize drug efficacy and selectivity.
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