7-Chloro-1,2,3,4-tetrahydroquinoline
≥95%
- Product Code: 51332
CAS:
90562-35-9
Molecular Weight: | 167.64 g./mol | Molecular Formula: | C₉H₁₀ClN |
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EC Number: | MDL Number: | MFCD08544268 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure serves as a building block for developing compounds with potential biological activities, particularly in the creation of drugs targeting the central nervous system. It is often employed in the production of antipsychotic and antidepressant medications, where its tetrahydroquinoline core contributes to the desired pharmacological effects. Additionally, it finds use in research and development for designing novel molecules with potential anti-inflammatory, antimicrobial, or anticancer properties. Its versatility in chemical transformations makes it valuable for creating diverse drug candidates.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,647.00 |
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0.250 | 10-20 days | ฿2,475.00 |
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1.000 | 10-20 days | ฿4,950.00 |
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5.000 | 10-20 days | ฿15,642.00 |
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7-Chloro-1,2,3,4-tetrahydroquinoline
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various therapeutic agents. Its structure serves as a building block for developing compounds with potential biological activities, particularly in the creation of drugs targeting the central nervous system. It is often employed in the production of antipsychotic and antidepressant medications, where its tetrahydroquinoline core contributes to the desired pharmacological effects. Additionally, it finds use in research and development for designing novel molecules with potential anti-inflammatory, antimicrobial, or anticancer properties. Its versatility in chemical transformations makes it valuable for creating diverse drug candidates.
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