2-Chloro-4-(naphthalen-2-yl)quinazoline

97%

Reagent Code: #165899
fingerprint
CAS Number 124959-44-0

science Other reagents with same CAS 124959-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.75 g/mol
Formula C₁₈H₁₁ClN₂
badge Registry Numbers
MDL Number MFCD32065726
thermostat Physical Properties
Melting Point 158-160 °C
Boiling Point 426.7±38.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.313±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to interact with biological targets through π-π stacking and hydrophobic interactions. Also employed in research settings to design novel quinazoline-based derivatives with potential antitumor and anti-inflammatory activities. Its structural framework is valuable in optimizing drug candidates for improved binding affinity and metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,280.00
inventory 250mg
10-20 days ฿12,370.00
inventory 1g
10-20 days ฿40,940.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Chloro-4-(naphthalen-2-yl)quinazoline
No image available

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to interact with biological targets through π-π stacking and hydrophobic interactions. Also employed in research settings to design novel quinazoline-based derivatives with potential antitumor and anti-inflammatory activities. Its structural framework is valuable in optimizing drug candidate

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to interact with biological targets through π-π stacking and hydrophobic interactions. Also employed in research settings to design novel quinazoline-based derivatives with potential antitumor and anti-inflammatory activities. Its structural framework is valuable in optimizing drug candidates for improved binding affinity and metabolic stability.

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...