5'-Bromospiro[cyclopropane-1,3'-indolin]-2'-one
95%
- Product Code: 75618
CAS:
875071-97-9
| Molecular Weight: | 238.08 g./mol | Molecular Formula: | C₁₀H₈BrNO |
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| EC Number: | MDL Number: | MFCD13195328 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed and dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of complex molecules. Its unique structure, featuring a bromine atom and a spirocyclic framework, makes it valuable for constructing indole-based compounds, which are often found in pharmaceuticals and agrochemicals. Researchers employ it in the synthesis of potential drug candidates, particularly those targeting neurological disorders and cancer, due to its ability to modulate biological pathways. Additionally, it is used in the creation of fluorescent dyes and imaging agents, aiding in biological studies and diagnostic applications. Its versatility in chemical reactions, such as cross-coupling and cyclization, further enhances its importance in advanced material science and medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $88.81 |
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| 0.250 | 10-20 days | $151.82 |
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| 1.000 | 10-20 days | $495.05 |
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| 5.000 | 10-20 days | $1,749.17 |
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5'-Bromospiro[cyclopropane-1,3'-indolin]-2'-one
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of complex molecules. Its unique structure, featuring a bromine atom and a spirocyclic framework, makes it valuable for constructing indole-based compounds, which are often found in pharmaceuticals and agrochemicals. Researchers employ it in the synthesis of potential drug candidates, particularly those targeting neurological disorders and cancer, due to its ability to modulate biological pathways. Additionally, it is used in the creation of fluorescent dyes and imaging agents, aiding in biological studies and diagnostic applications. Its versatility in chemical reactions, such as cross-coupling and cyclization, further enhances its importance in advanced material science and medicinal chemistry.
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