6-Bromo-2,3-dichloroquinoxaline

95%

Reagent Code: #146739
fingerprint
CAS Number 108229-82-9

science Other reagents with same CAS 108229-82-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.93 g/mol
Formula C₈H₃BrCl₂N₂
badge Registry Numbers
MDL Number MFCD09842518
thermostat Physical Properties
Boiling Point 326.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and antimicrobial agents. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to design compounds with biological activity, including antitumor and anti-inflammatory candidates. Also utilized in the preparation of organic semiconductors due to its electron-deficient aromatic core, contributing to materials with enhanced charge transport properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,840.00
inventory 250mg
10-20 days ฿3,410.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Bromo-2,3-dichloroquinoxaline
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and antimicrobial agents. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to design compounds with biological activity, including antitumor and anti-inflammatory candidates. Also utilized in the preparation of organic semicon

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and antimicrobial agents. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex heterocyclic systems. Commonly employed in research settings to design compounds with biological activity, including antitumor and anti-inflammatory candidates. Also utilized in the preparation of organic semiconductors due to its electron-deficient aromatic core, contributing to materials with enhanced charge transport properties.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...