Methyl 4-chloro-1H-indole-3-carboxylate
97%
- Product Code: 83909
CAS:
101909-42-6
Molecular Weight: | 209.63 g./mol | Molecular Formula: | C₁₀H₈ClNO₂ |
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EC Number: | MDL Number: | MFCD09841616 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
Methyl 4-chloro-1H-indole-3-carboxylate is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex indole derivatives. Its structure makes it a valuable building block in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential biological activity. This chemical is often employed in the preparation of molecules that may exhibit antimicrobial, anti-inflammatory, or anticancer properties. Additionally, it serves as a key precursor in the study of indole-based compounds, which are significant in medicinal chemistry due to their presence in many natural products and drugs. Researchers also use it to explore novel chemical reactions and pathways, contributing to advancements in synthetic methodologies.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | £27.48 |
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0.250 | 10-20 days | £55.57 |
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1.000 | 10-20 days | £157.75 |
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Methyl 4-chloro-1H-indole-3-carboxylate
Methyl 4-chloro-1H-indole-3-carboxylate is primarily utilized in organic synthesis as a versatile intermediate for the development of more complex indole derivatives. Its structure makes it a valuable building block in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential biological activity. This chemical is often employed in the preparation of molecules that may exhibit antimicrobial, anti-inflammatory, or anticancer properties. Additionally, it serves as a key precursor in the study of indole-based compounds, which are significant in medicinal chemistry due to their presence in many natural products and drugs. Researchers also use it to explore novel chemical reactions and pathways, contributing to advancements in synthetic methodologies.
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