6-Chloro-1,3-benzoxazol-2-amine

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Reagent Code: #159745
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CAS Number 52112-68-2

science Other reagents with same CAS 52112-68-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.58 g/mol
Formula C₇H₅ClN₂O
badge Registry Numbers
MDL Number MFCD01664218
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antiviral, antibacterial, and anti-inflammatory properties. Its structure serves as a core scaffold in medicinal chemistry for designing enzyme inhibitors and receptor modulators. Also employed in the preparation of agrochemicals and functional materials due to its stability and reactivity in coupling reactions. Commonly utilized in research settings for constructing benzoxazole-based derivatives with tailored biological activities.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿730.00
inventory 5g
10-20 days ฿3,290.00
inventory 25g
10-20 days ฿16,180.00

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6-Chloro-1,3-benzoxazol-2-amine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antiviral, antibacterial, and anti-inflammatory properties. Its structure serves as a core scaffold in medicinal chemistry for designing enzyme inhibitors and receptor modulators. Also employed in the preparation of agrochemicals and functional materials due to its stability and reactivity in coupling reactions. Commonly utilized in research settings for constructing benzoxaz

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive compounds with potential antiviral, antibacterial, and anti-inflammatory properties. Its structure serves as a core scaffold in medicinal chemistry for designing enzyme inhibitors and receptor modulators. Also employed in the preparation of agrochemicals and functional materials due to its stability and reactivity in coupling reactions. Commonly utilized in research settings for constructing benzoxazole-based derivatives with tailored biological activities.

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