6-Chloro-3,4-dihydroquinoxalin-2(1H)-one 6-Chloro-3,4-dihydroquinoxalin-2(1H)-one
95%
- Product Code: 120595
CAS:
89938-22-7
Molecular Weight: | 182.61 g./mol | Molecular Formula: | C₈H₇ClN₂O |
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EC Number: | MDL Number: | MFCD11520851 | |
Melting Point: | Boiling Point: | 386.8 °C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structural framework is often incorporated into the development of compounds targeting central nervous system disorders, such as anxiety and depression, due to its ability to interact with specific neurotransmitter systems. Additionally, it serves as a building block in the creation of potential antitumor agents, where its quinoxaline core is modified to enhance cytotoxic activity against cancer cells. Researchers also explore its derivatives for antimicrobial properties, aiming to combat resistant bacterial strains. Its versatility in drug discovery makes it a valuable scaffold for designing novel therapeutic agents.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿13,734.00 |
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1.000 | 10-20 days | ฿27,468.00 |
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6-Chloro-3,4-dihydroquinoxalin-2(1H)-one 6-Chloro-3,4-dihydroquinoxalin-2(1H)-one
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structural framework is often incorporated into the development of compounds targeting central nervous system disorders, such as anxiety and depression, due to its ability to interact with specific neurotransmitter systems. Additionally, it serves as a building block in the creation of potential antitumor agents, where its quinoxaline core is modified to enhance cytotoxic activity against cancer cells. Researchers also explore its derivatives for antimicrobial properties, aiming to combat resistant bacterial strains. Its versatility in drug discovery makes it a valuable scaffold for designing novel therapeutic agents.
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