2,4-dichloro-5-methylquinazoline

≥95%

Reagent Code: #178103
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CAS Number 78052-20-7

science Other reagents with same CAS 78052-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.06 g/mol
Formula C₉H₆Cl₂N₂
badge Registry Numbers
MDL Number MFCD11047029
thermostat Physical Properties
Boiling Point 292.4±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.418±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to undergo selective substitutions at specific positions. Commonly employed in research settings for designing compounds with antitumor, anti-inflammatory, and antimicrobial activities. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,770.00

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2,4-dichloro-5-methylquinazoline
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to undergo selective substitutions at specific positions. Commonly employed in research settings for designing compounds with antitumor, anti-inflammatory, and antimicrobial activities. Its structure allows for easy modification, making it valuable in medicinal chemistry for struct

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of bioactive molecules due to its ability to undergo selective substitutions at specific positions. Commonly employed in research settings for designing compounds with antitumor, anti-inflammatory, and antimicrobial activities. Its structure allows for easy modification, making it valuable in medicinal chemistry for structure-activity relationship studies.

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