(S)-1-(4-Bromothiophen-2-yl)ethan-1-amine
95%
- Product Code: 126379
CAS:
1213382-91-2
| Molecular Weight: | 206.10 g./mol | Molecular Formula: | C6H8BrNS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09822173 | |
| Melting Point: | Boiling Point: | 258.1±25.0 °C(Predicted) | |
| Density: | 1.557±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a bromothiophene moiety and an amine group, makes it a valuable intermediate in the development of biologically active compounds, particularly in the creation of drugs targeting neurological disorders or as part of medicinal chemistry projects. Additionally, it can be employed in asymmetric synthesis to produce enantiomerically pure substances, which are crucial in the development of therapeutics with high specificity and reduced side effects. Its application extends to material science, where it may be used in the design of organic semiconductors or conductive polymers due to the electronic properties of the thiophene ring.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $847.19 |
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| 0.250 | 10-20 days | $1,268.71 |
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(S)-1-(4-Bromothiophen-2-yl)ethan-1-amine
This compound is primarily utilized in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a bromothiophene moiety and an amine group, makes it a valuable intermediate in the development of biologically active compounds, particularly in the creation of drugs targeting neurological disorders or as part of medicinal chemistry projects. Additionally, it can be employed in asymmetric synthesis to produce enantiomerically pure substances, which are crucial in the development of therapeutics with high specificity and reduced side effects. Its application extends to material science, where it may be used in the design of organic semiconductors or conductive polymers due to the electronic properties of the thiophene ring.
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