Ethyl 2-chloro-1H-benzo[d]imidazole-6-carboxylate

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Reagent Code: #183510
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CAS Number 857035-29-1

science Other reagents with same CAS 857035-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 224.64 g/mol
Formula C₁₀H₉ClN₂O₂
badge Registry Numbers
MDL Number MFCD12827540
thermostat Physical Properties
Boiling Point 401.4±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its structure supports the formation of biologically active benzimidazole derivatives, which are known for their interaction with cellular enzymes and receptors. Commonly employed in medicinal chemistry for constructing drug candidates targeting gastrointestinal disorders, hypertension, and infectious diseases. Also utilized in agrochemical research for designing new active ingredients in crop protection agents due to its stability and reactivity in various coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,020.00
inventory 100mg
10-20 days ฿1,610.00
inventory 250mg
10-20 days ฿3,420.00
inventory 1g
10-20 days ฿10,300.00
inventory 5g
10-20 days ฿38,160.00

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Ethyl 2-chloro-1H-benzo[d]imidazole-6-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its structure supports the formation of biologically active benzimidazole derivatives, which are known for their interaction with cellular enzymes and receptors. Commonly employed in medicinal chemistry for constructing drug candidates targeting gastrointestinal disorders, hypertension, and infectious diseases. Also utilized in agrochemical research for designing new acti

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antiparasitic and antiviral agents. Its structure supports the formation of biologically active benzimidazole derivatives, which are known for their interaction with cellular enzymes and receptors. Commonly employed in medicinal chemistry for constructing drug candidates targeting gastrointestinal disorders, hypertension, and infectious diseases. Also utilized in agrochemical research for designing new active ingredients in crop protection agents due to its stability and reactivity in various coupling reactions.

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