2, 4-Dichloro-6-(trifluoromethyl)quinazoline

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Reagent Code: #177944
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CAS Number 864291-30-5

science Other reagents with same CAS 864291-30-5

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scatter_plot Molecular Information
Weight 267.03 g/mol
Formula C₉H₃Cl₂F₃N₂
badge Registry Numbers
MDL Number MFCD09954876
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

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 agrochemicals for the production of herbicides and pesticides due to its stable heterocyclic structure and reactive halogen sites. Its trifluoromethyl and chloro substituents enhance lipophilicity and bioavailability, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research for designing novel compounds with antimicrobial or anti-inflammatory activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,800.00
inventory 250mg
10-20 days ฿9,900.00
inventory 1g
10-20 days ฿25,650.00

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2, 4-Dichloro-6-(trifluoromethyl)quinazoline
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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 agrochemicals for the production of herbicides and pesticides due to its stable heterocyclic structure and reactive halogen sites. Its trifluoromethyl and chloro substituents enhance lipophilicity and bioavailability, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research for designing novel co

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 agrochemicals for the production of herbicides and pesticides due to its stable heterocyclic structure and reactive halogen sites. Its trifluoromethyl and chloro substituents enhance lipophilicity and bioavailability, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in research for designing novel compounds with antimicrobial or anti-inflammatory activity.

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