3-Bromoquinoline-6-carbonitrile

98%

Reagent Code: #65568
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CAS Number 205114-19-8

science Other reagents with same CAS 205114-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.06 g/mol
Formula C₁₀H₅BrN₂
badge Registry Numbers
MDL Number MFCD28334791
thermostat Physical Properties
Boiling Point 358.7±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.66±0.1 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity, such as inhibitors for various enzymes. Its structure is valuable in creating heterocyclic compounds, which are often explored for their therapeutic properties. Additionally, it is utilized in research for designing new drugs targeting diseases like cancer, inflammation, and infections. The bromine substituent enables nucleophilic substitution reactions, and the nitrile group supports carbon-carbon bond formations, making it a versatile building block for further chemical modifications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,350.00
inventory 250mg
10-20 days ฿27,720.00
inventory 1g
10-20 days ฿72,000.00

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3-Bromoquinoline-6-carbonitrile
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Used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity, such as inhibitors for various enzymes. Its structure is valuable in creating heterocyclic compounds, which are often explored for their therapeutic properties. Additionally, it is utilized in research for designing new drugs targeting diseases like cancer, inflammation, and infections. The bromine substituent e

Used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity, such as inhibitors for various enzymes. Its structure is valuable in creating heterocyclic compounds, which are often explored for their therapeutic properties. Additionally, it is utilized in research for designing new drugs targeting diseases like cancer, inflammation, and infections. The bromine substituent enables nucleophilic substitution reactions, and the nitrile group supports carbon-carbon bond formations, making it a versatile building block for further chemical modifications.

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