3-Isoquinolinecarboxylic acid, 6-bromo-1-chloro-, methyl ester

95%

Reagent Code: #198715
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CAS Number 1600855-21-7

science Other reagents with same CAS 1600855-21-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.5358 g/mol
Formula C₁₁H₇BrClNO₂
thermostat Physical Properties
Boiling Point 436.1±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.644±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of complex heterocyclic systems found in certain anticancer and anti-inflammatory agents. The bromo and chloro substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent probes and imaging agents due to the isoquinoline core’s photophysical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿24,000.00
inventory 500mg
10-20 days ฿35,200.00
inventory 1g
10-20 days ฿46,400.00

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3-Isoquinolinecarboxylic acid, 6-bromo-1-chloro-, methyl ester
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of complex heterocyclic systems found in certain anticancer and anti-inflammatory agents. The bromo and chloro substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent probes and imag

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its structure supports the construction of complex heterocyclic systems found in certain anticancer and anti-inflammatory agents. The bromo and chloro substituents allow for further functionalization via cross-coupling reactions, making it valuable in medicinal chemistry research. Also employed in the preparation of fluorescent probes and imaging agents due to the isoquinoline core’s photophysical properties.

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