tert-Butyl (7-bromoisoquinolin-3-yl)carbamate

≥97%

Reagent Code: #37123
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CAS Number 2089301-09-5

science Other reagents with same CAS 2089301-09-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.19 g/mol
Formula C₁₄H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD30188704
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It plays a role in the preparation of isoquinoline derivatives, which are studied for their biological activities, including anticancer, anti-inflammatory, and antimicrobial effects. The bromine atom in the structure allows for further functionalization through cross-coupling reactions, enabling the synthesis of complex molecules. This compound is also utilized in research focused on drug discovery and medicinal chemistry to explore novel bioactive agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,360.00
inventory 250mg
10-20 days ฿24,710.00

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tert-Butyl (7-bromoisoquinolin-3-yl)carbamate
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Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It plays a role in the preparation of isoquinoline derivatives, which are studied for their biological activities, including anticancer, anti-inflammatory, and antimicrobial effects. The bromine atom in the structure allows for further functionalization through cross-coupling reactions, enabling the synthesis of complex molecules. This compo
Used in organic synthesis as a key intermediate for the development of pharmaceuticals, particularly in the creation of compounds with potential therapeutic properties. It plays a role in the preparation of isoquinoline derivatives, which are studied for their biological activities, including anticancer, anti-inflammatory, and antimicrobial effects. The bromine atom in the structure allows for further functionalization through cross-coupling reactions, enabling the synthesis of complex molecules. This compound is also utilized in research focused on drug discovery and medicinal chemistry to explore novel bioactive agents.
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