Ethyl 5-(3,4-difluorophenyl)-3-methyl-1H-pyrrole-2-carboxylate
97%
- Product Code: 48169
CAS:
2106792-88-3
Molecular Weight: | 265.26 g./mol | Molecular Formula: | C₁₄H₁₃F₂NO₂ |
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Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of pharmaceutical agents, particularly those targeting central nervous system disorders. Its structure, featuring a pyrrole ring and difluorophenyl group, makes it a valuable building block for designing compounds with potential biological activity. Researchers explore its use in creating novel drugs that may exhibit anti-inflammatory, analgesic, or neuroprotective properties. Additionally, it serves as a key precursor in the preparation of heterocyclic compounds, which are widely studied for their therapeutic applications. Its versatility in chemical reactions also makes it a useful tool in organic synthesis for constructing diverse molecular frameworks.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,075.00 |
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0.250 | 10-20 days | ฿12,150.00 |
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Ethyl 5-(3,4-difluorophenyl)-3-methyl-1H-pyrrole-2-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of pharmaceutical agents, particularly those targeting central nervous system disorders. Its structure, featuring a pyrrole ring and difluorophenyl group, makes it a valuable building block for designing compounds with potential biological activity. Researchers explore its use in creating novel drugs that may exhibit anti-inflammatory, analgesic, or neuroprotective properties. Additionally, it serves as a key precursor in the preparation of heterocyclic compounds, which are widely studied for their therapeutic applications. Its versatility in chemical reactions also makes it a useful tool in organic synthesis for constructing diverse molecular frameworks.
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