2-Chloro-6,7-difluoroquinoxaline

98%

Reagent Code: #166496
fingerprint
CAS Number 143007-15-2

science Other reagents with same CAS 143007-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.57 g/mol
Formula C₈H₃ClF₂N₂
badge Registry Numbers
MDL Number MFCD11518958
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the design of compounds with high selectivity and potency in targeting specific signaling pathways. Commonly employed in medicinal chemistry for constructing biologically active quinoxaline derivatives. Also utilized in research settings to develop new agrochemicals and functional materials due to its electron-deficient aromatic core, which enhances reactivity in cross-coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,190.00
inventory 250mg
10-20 days ฿10,320.00
inventory 1g
10-20 days ฿25,780.00
inventory 5g
10-20 days ฿58,630.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Chloro-6,7-difluoroquinoxaline
No image available

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the design of compounds with high selectivity and potency in targeting specific signaling pathways. Commonly employed in medicinal chemistry for constructing biologically active quinoxaline derivatives. Also utilized in research settings to develop new agrochemicals and functional materials due to its electron-deficient aromatic core, which enhances reac

Used in the synthesis of pharmaceutical intermediates, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports the design of compounds with high selectivity and potency in targeting specific signaling pathways. Commonly employed in medicinal chemistry for constructing biologically active quinoxaline derivatives. Also utilized in research settings to develop new agrochemicals and functional materials due to its electron-deficient aromatic core, which enhances reactivity in cross-coupling reactions.

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...