1-Chloroisoquinoline-4-carbonitrile
≥95%
- Product Code: 114702
CAS:
53491-80-8
| Molecular Weight: | 188.61 g./mol | Molecular Formula: | C₁₀H₅ClN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13193485 | |
| Melting Point: | Boiling Point: | 355.247°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
1-Chloroisoquinoline-4-carbonitrile is primarily utilized in the field of organic synthesis as a versatile building block for the development of complex molecules. Its structure, featuring both a chloro and a nitrile group, makes it a valuable intermediate in the synthesis of various heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the preparation of pharmaceuticals, particularly in the design of drug candidates targeting specific enzymes or receptors. Its reactivity also allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and material science applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,825.00 |
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| 0.250 | 10-20 days | ฿6,084.00 |
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| 1.000 | 10-20 days | ฿15,309.00 |
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1-Chloroisoquinoline-4-carbonitrile
1-Chloroisoquinoline-4-carbonitrile is primarily utilized in the field of organic synthesis as a versatile building block for the development of complex molecules. Its structure, featuring both a chloro and a nitrile group, makes it a valuable intermediate in the synthesis of various heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it serves as a precursor in the preparation of pharmaceuticals, particularly in the design of drug candidates targeting specific enzymes or receptors. Its reactivity also allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and material science applications.
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