5-(trifluoromethyl)-N2-methylpyridine-2,3-diamine

≥95%

Reagent Code: #216917
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CAS Number 172648-55-4

science Other reagents with same CAS 172648-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.15 g/mol
Formula C₇H₈F₃N₃
badge Registry Numbers
MDL Number MFCD00068119
thermostat Physical Properties
Melting Point 99-101 °C
Boiling Point 285.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Commonly employed in kinase inhibitor research due to its ability to improve binding affinity and selectivity. Also utilized in the preparation of pyrido[2,3-d]pyrimidine derivatives with potential antitumor and anti-inflammatory activities.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,840.00
inventory 25g
10-20 days ฿8,840.00

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5-(trifluoromethyl)-N2-methylpyridine-2,3-diamine
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Commonly employed in kinase inhibitor research due to its ability to improve binding affinity and selectivity. Also utilized in the preparation of pyrido[2,3-d]pyrimidine derivatives with potential antitumor and anti-inflammatory activiti

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its trifluoromethyl group enhances lipophilicity and metabolic stability, making it valuable in designing bioactive molecules. Commonly employed in kinase inhibitor research due to its ability to improve binding affinity and selectivity. Also utilized in the preparation of pyrido[2,3-d]pyrimidine derivatives with potential antitumor and anti-inflammatory activities.

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