(1H-Benzimidazol-2-ylmethyl)methylamine dihydrochloride

≥95%

Reagent Code: #197801
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CAS Number 92809-96-6

science Other reagents with same CAS 92809-96-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.12 g/mol
Formula C₉H₁₃Cl₂N₃
badge Registry Numbers
MDL Number MFCD07161795
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs. It serves as a building block for compounds with antiparasitic, antiviral, and anticancer activities. Its structure allows for easy modification in drug design, making it valuable in medicinal chemistry research. Commonly employed in the preparation of proton pump inhibitors and anthelmintic agents due to the benzimidazole core’s affinity for biological targets. Also utilized in the creation of ligands for metal-catalyzed reactions in organic synthesis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿23,660.00
(1H-Benzimidazol-2-ylmethyl)methylamine dihydrochloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs. It serves as a building block for compounds with antiparasitic, antiviral, and anticancer activities. Its structure allows for easy modification in drug design, making it valuable in medicinal chemistry research. Commonly employed in the preparation of proton pump inhibitors and anthelmintic agents due to the benzimidazole core’s affinity for biological targets. Also utiliz

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs. It serves as a building block for compounds with antiparasitic, antiviral, and anticancer activities. Its structure allows for easy modification in drug design, making it valuable in medicinal chemistry research. Commonly employed in the preparation of proton pump inhibitors and anthelmintic agents due to the benzimidazole core’s affinity for biological targets. Also utilized in the creation of ligands for metal-catalyzed reactions in organic synthesis.

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