5-Methoxyisoquinoline Hydrochloride

≥97%

Reagent Code: #207739
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CAS Number 1418117-87-9

science Other reagents with same CAS 1418117-87-9

blur_circular Chemical Specifications

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Weight 195.65 g/mol
Formula C₁₀H₁₀ClNO
inventory_2 Storage & Handling
Storage Room temperature, dryness, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antipsychotic drugs. It serves as a building block in the preparation of isoquinoline-based bioactive molecules due to its ability to participate in various coupling and substitution reactions. Its methoxy-substituted structure enhances electron density, improving reactivity in catalytic reactions and enabling selective functionalization. Commonly employed in research settings for designing novel therapeutic compounds with improved metabolic stability and binding affinity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,220.00
inventory 5g
10-20 days ฿10,270.00

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5-Methoxyisoquinoline Hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antipsychotic drugs. It serves as a building block in the preparation of isoquinoline-based bioactive molecules due to its ability to participate in various coupling and substitution reactions. Its methoxy-substituted structure enhances electron density, improving reactivity in catalytic reactions and enabling selective functionalization. Commonly employed in research setti

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system agents and antipsychotic drugs. It serves as a building block in the preparation of isoquinoline-based bioactive molecules due to its ability to participate in various coupling and substitution reactions. Its methoxy-substituted structure enhances electron density, improving reactivity in catalytic reactions and enabling selective functionalization. Commonly employed in research settings for designing novel therapeutic compounds with improved metabolic stability and binding affinity.

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