3,5-Dichloro-4-(trifluoromethyl)pyridin-2-amine

95%

Reagent Code: #179774
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CAS Number 1446182-76-8

science Other reagents with same CAS 1446182-76-8

blur_circular Chemical Specifications

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Weight 231.00 g/mol
Formula C₆H₃Cl₂F₃N₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure supports the creation of active ingredients with enhanced selectivity and stability. The compound’s electron-withdrawing groups improve bioavailability and resistance to metabolic degradation, making it valuable in crop protection agents. It also serves in research for novel kinase inhibitors and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,390.00
inventory 250mg
10-20 days ฿15,690.00
inventory 1g
10-20 days ฿39,210.00

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3,5-Dichloro-4-(trifluoromethyl)pyridin-2-amine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure supports the creation of active ingredients with enhanced selectivity and stability. The compound’s electron-withdrawing groups improve bioavailability and resistance to metabolic degradation, making it valuable in crop protection agents. It also serves in research for novel kinase inhibitors and antimicrobial agents due to its ability to interact with

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure supports the creation of active ingredients with enhanced selectivity and stability. The compound’s electron-withdrawing groups improve bioavailability and resistance to metabolic degradation, making it valuable in crop protection agents. It also serves in research for novel kinase inhibitors and antimicrobial agents due to its ability to interact with biological targets through hydrogen bonding and hydrophobic interactions.

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