string(7) "reagent" 2-Chloroquinolin-7-ol

2-Chloroquinolin-7-ol

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Reagent Code: #124075
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CAS Number 375358-19-3

science Other reagents with same CAS 375358-19-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.6 g/mol
Formula C₉H₆ClNO
badge Registry Numbers
MDL Number MFCD02238180
thermostat Physical Properties
Boiling Point 342 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, particularly in the development of antimalarial and antimicrobial agents. Its structure is valuable in creating quinoline derivatives, which are explored for their potential therapeutic properties. Additionally, it finds application in the synthesis of dyes and agrochemicals due to its reactive chloroquinoline backbone. Researchers also utilize it in the study of chemical reactions and mechanisms involving halogenated heterocycles.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿35,118.00
inventory 1g
10-20 days ฿9,432.00
inventory 250mg
10-20 days ฿3,717.00

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2-Chloroquinolin-7-ol
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, particularly in the development of antimalarial and antimicrobial agents. Its structure is valuable in creating quinoline derivatives, which are explored for their potential therapeutic properties. Additionally, it finds application in the synthesis of dyes and agrochemicals due to its reactive chloroquinoline backbone. Researchers also utilize it in the study of chemical reactions and me

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of pharmaceuticals, particularly in the development of antimalarial and antimicrobial agents. Its structure is valuable in creating quinoline derivatives, which are explored for their potential therapeutic properties. Additionally, it finds application in the synthesis of dyes and agrochemicals due to its reactive chloroquinoline backbone. Researchers also utilize it in the study of chemical reactions and mechanisms involving halogenated heterocycles.

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