tert-Butyl (4-chloroquinolin-6-yl)carbamate

98%

Reagent Code: #36902
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CAS Number 1447606-50-9

science Other reagents with same CAS 1447606-50-9

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Weight 278.73 g/mol
Formula C₁₄H₁₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD25542348
inventory_2 Storage & Handling
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description Product Description

Used primarily in organic synthesis, this compound serves as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of quinoline-based drugs, which have applications in treating malaria, cancer, and other diseases. The tert-butyl group provides stability and aids in protecting functional groups during multi-step synthetic processes. Additionally, its chloroquinoline moiety is valuable for creating compounds with potential antimicrobial and anti-inflammatory properties. Researchers also utilize it in the study of enzyme inhibition and receptor binding activities.

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inventory 100mg
10-20 days ฿8,631.00

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tert-Butyl (4-chloroquinolin-6-yl)carbamate
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Used primarily in organic synthesis, this compound serves as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of quinoline-based drugs, which have applications in treating malaria, cancer, and other diseases. The tert-butyl group provides stability and aids in protecting functional groups during multi-step synthetic processes. Additionally, its chloroquinoline moiety is valuable for creating compounds with potent

Used primarily in organic synthesis, this compound serves as an intermediate in the production of more complex molecules, particularly in pharmaceutical research. It is often employed in the development of quinoline-based drugs, which have applications in treating malaria, cancer, and other diseases. The tert-butyl group provides stability and aids in protecting functional groups during multi-step synthetic processes. Additionally, its chloroquinoline moiety is valuable for creating compounds with potential antimicrobial and anti-inflammatory properties. Researchers also utilize it in the study of enzyme inhibition and receptor binding activities.

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