3-Bromo-1,6-naphthyridine

97%

Reagent Code: #117922
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CAS Number 17965-73-0

science Other reagents with same CAS 17965-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.59 g/mol
Formula C₅H₈ClN₃O₂
badge Registry Numbers
MDL Number MFCD22040108
thermostat Physical Properties
Boiling Point 306.2±22.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

3-Bromo-1,6-naphthyridine is primarily used in organic synthesis as a versatile intermediate for constructing more complex chemical structures. Its bromine atom serves as a reactive site, enabling cross-coupling reactions such as Suzuki or Buchwald-Hartwig reactions, which are essential in pharmaceutical and materials research. This compound is particularly valuable in the development of heterocyclic compounds, which are often explored for their potential biological activities, including antimicrobial, anticancer, or antiviral properties. Additionally, it finds application in the synthesis of organic electronic materials, where its naphthyridine core contributes to the development of light-emitting or charge-transporting molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,980.00
inventory 250mg
10-20 days ฿17,604.00
inventory 1g
10-20 days ฿44,100.00
3-Bromo-1,6-naphthyridine
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3-Bromo-1,6-naphthyridine is primarily used in organic synthesis as a versatile intermediate for constructing more complex chemical structures. Its bromine atom serves as a reactive site, enabling cross-coupling reactions such as Suzuki or Buchwald-Hartwig reactions, which are essential in pharmaceutical and materials research. This compound is particularly valuable in the development of heterocyclic compounds, which are often explored for their potential biological activities, including antimicrobial, a

3-Bromo-1,6-naphthyridine is primarily used in organic synthesis as a versatile intermediate for constructing more complex chemical structures. Its bromine atom serves as a reactive site, enabling cross-coupling reactions such as Suzuki or Buchwald-Hartwig reactions, which are essential in pharmaceutical and materials research. This compound is particularly valuable in the development of heterocyclic compounds, which are often explored for their potential biological activities, including antimicrobial, anticancer, or antiviral properties. Additionally, it finds application in the synthesis of organic electronic materials, where its naphthyridine core contributes to the development of light-emitting or charge-transporting molecules.

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