2-(6-chloro-1H-benzimidazol-2-yl)ethanamine

95%

Reagent Code: #196496
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CAS Number 135875-16-0

science Other reagents with same CAS 135875-16-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 195.65 g/mol
Formula C₉H₁₀ClN₃
badge Registry Numbers
MDL Number MFCD08691444
thermostat Physical Properties
Boiling Point 432.1±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.363±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, inert atmosphere

description Product Description

Used in the synthesis of pharmaceutical agents, particularly in developing anthelmintic and antiparasitic drugs. Its structure supports activity against gastrointestinal parasites by interfering with tubulin polymerization in worm cells. Also serves as an intermediate in creating bioactive molecules for research in neuropharmacology due to the amine functionality enabling blood-brain barrier penetration. Employed in studies exploring treatments for protozoal infections and as a building block in medicinal chemistry for designing novel benzimidazole derivatives with improved efficacy and reduced resistance.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,200.00
250mg
10-20 days ฿3,670.00
1g
10-20 days ฿9,020.00
2-(6-chloro-1H-benzimidazol-2-yl)ethanamine
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Used in the synthesis of pharmaceutical agents, particularly in developing anthelmintic and antiparasitic drugs. Its structure supports activity against gastrointestinal parasites by interfering with tubulin polymerization in worm cells. Also serves as an intermediate in creating bioactive molecules for research in neuropharmacology due to the amine functionality enabling blood-brain barrier penetration. Employed in studies exploring treatments for protozoal infections and as a building block in medicina

Used in the synthesis of pharmaceutical agents, particularly in developing anthelmintic and antiparasitic drugs. Its structure supports activity against gastrointestinal parasites by interfering with tubulin polymerization in worm cells. Also serves as an intermediate in creating bioactive molecules for research in neuropharmacology due to the amine functionality enabling blood-brain barrier penetration. Employed in studies exploring treatments for protozoal infections and as a building block in medicinal chemistry for designing novel benzimidazole derivatives with improved efficacy and reduced resistance.

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