3-Bromo-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid
96%
- Product Code: 45347
CAS:
1823918-84-8
| Molecular Weight: | 241.0415 g./mol | Molecular Formula: | C₈H₅BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD28098153 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. It serves as a building block for the development of pharmaceutical agents, particularly in the design of small molecule inhibitors targeting specific enzymes or receptors. Its pyrrolo[1,2-a]pyrimidine core structure is often incorporated into molecules with potential therapeutic applications, such as anti-cancer, anti-inflammatory, or antiviral drugs. Additionally, it is employed in research settings for the exploration of structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Its bromo substituent allows for further functionalization through various coupling reactions, making it a versatile component in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $468.50 |
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3-Bromo-pyrrolo[1,2-a]pyrimidine-6-carboxylic acid
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. It serves as a building block for the development of pharmaceutical agents, particularly in the design of small molecule inhibitors targeting specific enzymes or receptors. Its pyrrolo[1,2-a]pyrimidine core structure is often incorporated into molecules with potential therapeutic applications, such as anti-cancer, anti-inflammatory, or antiviral drugs. Additionally, it is employed in research settings for the exploration of structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Its bromo substituent allows for further functionalization through various coupling reactions, making it a versatile component in organic synthesis.
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