2-(Chloromethyl)-1-phenyl-1H-benzimidazole

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Reagent Code: #173066
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CAS Number 94937-86-7

science Other reagents with same CAS 94937-86-7

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scatter_plot Molecular Information
Weight 242.70 g/mol
Formula C₁₄H₁₁ClN₂
badge Registry Numbers
MDL Number MFCD04114570
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-derived drugs with antiparasitic, antiviral, and anticancer properties. Its reactive chloromethyl group allows for easy alkylation and functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in the preparation of proton pump inhibitors and anthelmintic agents. Also utilized in agrochemical research for developing new fungicides and plant growth regulators. Its versatility in nucleophilic substitution reactions enhances its role in medicinal chemistry and drug design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,683.00
inventory 1g
10-20 days ฿10,460.00
inventory 5g
10-20 days ฿30,930.00

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2-(Chloromethyl)-1-phenyl-1H-benzimidazole
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Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-derived drugs with antiparasitic, antiviral, and anticancer properties. Its reactive chloromethyl group allows for easy alkylation and functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in the preparation of proton pump inhibitors and anthelmintic agents. Also utilized in agrochemical research for developing new fungicides and plant gro

Used primarily as an intermediate in the synthesis of pharmaceuticals, particularly in the development of benzimidazole-derived drugs with antiparasitic, antiviral, and anticancer properties. Its reactive chloromethyl group allows for easy alkylation and functionalization, making it valuable in constructing complex heterocyclic systems. Commonly employed in the preparation of proton pump inhibitors and anthelmintic agents. Also utilized in agrochemical research for developing new fungicides and plant growth regulators. Its versatility in nucleophilic substitution reactions enhances its role in medicinal chemistry and drug design.

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