6-chloro-2-hydrazinopurine

95%

Reagent Code: #163264
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CAS Number 5404-88-6

science Other reagents with same CAS 5404-88-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.59 g/mol
Formula C₅H₅ClN₆
badge Registry Numbers
MDL Number MFCD19707218
thermostat Physical Properties
Boiling Point 332.9 °C at 760 mmHg
inventory_2 Storage & Handling
Density 2.15 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting purine metabolism. It serves as a key building block in the preparation of modified nucleosides and nucleotides, which are important in antiviral and anticancer drug research. Its hydrazino group allows for further functionalization, enabling the creation of diverse heterocyclic systems. Commonly employed in the production of cytokinin-type plant growth regulators due to its structural similarity to adenine derivatives involved in cell division. Also utilized in biochemical studies to probe enzyme mechanisms involving purine-binding sites.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,850.00
inventory 250mg
10-20 days ฿4,740.00
inventory 1g
10-20 days ฿9,490.00
inventory 5g
10-20 days ฿28,530.00

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6-chloro-2-hydrazinopurine
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Used primarily as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting purine metabolism. It serves as a key building block in the preparation of modified nucleosides and nucleotides, which are important in antiviral and anticancer drug research. Its hydrazino group allows for further functionalization, enabling the creation of diverse heterocyclic systems. Commonly employed in the production of cytokinin-type plant growth regulat

Used primarily as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting purine metabolism. It serves as a key building block in the preparation of modified nucleosides and nucleotides, which are important in antiviral and anticancer drug research. Its hydrazino group allows for further functionalization, enabling the creation of diverse heterocyclic systems. Commonly employed in the production of cytokinin-type plant growth regulators due to its structural similarity to adenine derivatives involved in cell division. Also utilized in biochemical studies to probe enzyme mechanisms involving purine-binding sites.

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