7-Chloro-6-nitro-4-hydroxyquinazoline
98%
- Product Code: 120839
CAS:
53449-14-2
Molecular Weight: | 225.59 g./mol | Molecular Formula: | C₈H₄ClN₃O₃ |
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EC Number: | MDL Number: | MFCD09388771 | |
Melting Point: | 314-319℃ | Boiling Point: | |
Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of quinazoline-based drugs, which are known for their therapeutic potential in treating a range of diseases. Specifically, it serves as a building block in the creation of inhibitors targeting specific enzymes or receptors involved in pathological processes. For instance, it has been explored in the design of compounds with anti-cancer properties, where it helps in modulating pathways critical to tumor growth and survival. Additionally, its derivatives have shown promise in the development of anti-inflammatory and antimicrobial agents, making it a versatile component in drug discovery and development efforts.
Product Specification:
Test | Specification |
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Purity (HPLC) | 98 |
Purity (Neutralization Titration) | 97.5-102.5 |
Melting Point | 314-319 |
Appearance | White To Yellow Or Brown Powder |
Infrared Spectrum | Conforms To Structure |
Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | €8.71 |
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5.000 | 10-20 days | €22.42 |
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25.000 | 10-20 days | €97.61 |
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100.000 | 10-20 days | €263.29 |
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7-Chloro-6-nitro-4-hydroxyquinazoline
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure is particularly valuable in the development of quinazoline-based drugs, which are known for their therapeutic potential in treating a range of diseases. Specifically, it serves as a building block in the creation of inhibitors targeting specific enzymes or receptors involved in pathological processes. For instance, it has been explored in the design of compounds with anti-cancer properties, where it helps in modulating pathways critical to tumor growth and survival. Additionally, its derivatives have shown promise in the development of anti-inflammatory and antimicrobial agents, making it a versatile component in drug discovery and development efforts.
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