(R)-1-(3-Chloropyridin-2-yl)-2,2,2-trifluoroethanamine hydrochloride

95%

Reagent Code: #230896
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CAS Number 2089671-65-6

science Other reagents with same CAS 2089671-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.05 g/mol
Formula C₇H₇Cl₂F₃N₂
badge Registry Numbers
MDL Number MFCD30828976
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of selective insecticides. Its structure supports enhanced binding affinity to target receptors in pests, improving efficacy at lower application rates. Also utilized in the development of pharmaceuticals due to its chiral stability and ability to influence biological activity in active ingredients. The compound’s trifluoromethyl group contributes to increased metabolic stability and environmental persistence, making it valuable in crop protection chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,400.00
inventory 250mg
10-20 days ฿22,800.00
inventory 1g
10-20 days ฿44,420.00

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(R)-1-(3-Chloropyridin-2-yl)-2,2,2-trifluoroethanamine hydrochloride
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of selective insecticides. Its structure supports enhanced binding affinity to target receptors in pests, improving efficacy at lower application rates. Also utilized in the development of pharmaceuticals due to its chiral stability and ability to influence biological activity in active ingredients. The compound’s trifluoromethyl group contributes to increased metabolic stability and environmental persistence, ma

Used as a key intermediate in the synthesis of agrochemicals, particularly in the production of selective insecticides. Its structure supports enhanced binding affinity to target receptors in pests, improving efficacy at lower application rates. Also utilized in the development of pharmaceuticals due to its chiral stability and ability to influence biological activity in active ingredients. The compound’s trifluoromethyl group contributes to increased metabolic stability and environmental persistence, making it valuable in crop protection chemistry.

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