4-CHLORO-6,7-DIMETHYLENEDIOXYQUINAZOLINE

≥95%

Reagent Code: #157219
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CAS Number 52791-05-6

science Other reagents with same CAS 52791-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.6278 g/mol
Formula C₁₀H₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD09838958
thermostat Physical Properties
Melting Point 216 °C
Boiling Point 375.4±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.475±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports binding to enzyme active sites, making it valuable in creating targeted treatments for tumors. Also employed in research settings to explore new pathways in cell signaling and apoptosis regulation. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,600.00
inventory 250mg
10-20 days ฿19,200.00

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4-CHLORO-6,7-DIMETHYLENEDIOXYQUINAZOLINE
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports binding to enzyme active sites, making it valuable in creating targeted treatments for tumors. Also employed in research settings to explore new pathways in cell signaling and apoptosis regulation. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer therapy. Its structure supports binding to enzyme active sites, making it valuable in creating targeted treatments for tumors. Also employed in research settings to explore new pathways in cell signaling and apoptosis regulation. Commonly utilized in medicinal chemistry for scaffold modification to enhance drug potency and selectivity.

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