(1-Benzyl-1H-benzo[d]imidazol-2-yl)methanol

≥98%

Reagent Code: #140845
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CAS Number 6646-70-4

science Other reagents with same CAS 6646-70-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.28 g/mol
Formula C₁₅H₁₄N₂O
badge Registry Numbers
MDL Number MFCD00182174
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs which exhibit antimicrobial, antiviral, and antifungal activities. It serves as a building block in creating compounds with potential use in treating gastrointestinal disorders, parasitic infections, and certain types of cancer. Its hydroxyl and benzyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of ligands for metal-catalyzed reactions in organic synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,930.00
inventory 25g
10-20 days ฿23,300.00
inventory 5g
10-20 days ฿6,670.00

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(1-Benzyl-1H-benzo[d]imidazol-2-yl)methanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs which exhibit antimicrobial, antiviral, and antifungal activities. It serves as a building block in creating compounds with potential use in treating gastrointestinal disorders, parasitic infections, and certain types of cancer. Its hydroxyl and benzyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-based drugs which exhibit antimicrobial, antiviral, and antifungal activities. It serves as a building block in creating compounds with potential use in treating gastrointestinal disorders, parasitic infections, and certain types of cancer. Its hydroxyl and benzyl functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in the preparation of ligands for metal-catalyzed reactions in organic synthesis.
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