2-Chloro-9H-purine

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Reagent Code: #160341
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CAS Number 1681-15-8

science Other reagents with same CAS 1681-15-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.56 g/mol
Formula C₅H₃ClN₄
thermostat Physical Properties
Boiling Point 397.7°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of purine-based drugs such as antiviral and anticancer agents. It serves as a building block for modifying the purine scaffold to develop biologically active compounds. Commonly employed in medicinal chemistry for nucleoside analog development, where selective substitution at the 2-position enhances target specificity and metabolic stability. Also utilized in research settings for labeling and probing nucleic acid interactions.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,020.00
inventory 1g
10-20 days ฿2,940.00
inventory 5g
10-20 days ฿12,280.00

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2-Chloro-9H-purine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of purine-based drugs such as antiviral and anticancer agents. It serves as a building block for modifying the purine scaffold to develop biologically active compounds. Commonly employed in medicinal chemistry for nucleoside analog development, where selective substitution at the 2-position enhances target specificity and metabolic stability. Also utilized in research settings for labeling and probing nucleic aci

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the preparation of purine-based drugs such as antiviral and anticancer agents. It serves as a building block for modifying the purine scaffold to develop biologically active compounds. Commonly employed in medicinal chemistry for nucleoside analog development, where selective substitution at the 2-position enhances target specificity and metabolic stability. Also utilized in research settings for labeling and probing nucleic acid interactions.

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