5-Iodopyrazin-2-amine

97%

Reagent Code: #199753
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CAS Number 886860-50-0

science Other reagents with same CAS 886860-50-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221 g/mol
Formula C₄H₄IN₃
thermostat Physical Properties
Melting Point 122-123°C
Boiling Point 337.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing biologically active molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays due to the presence of the iodine atom, which facilitates radiolabeling or serves as a handle for further derivatization.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,700.00
10g
10-20 days ฿2,840.00
25g
10-20 days ฿5,380.00
100g
10-20 days ฿18,620.00
5-Iodopyrazin-2-amine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing biologically active molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in the preparation of fluorescent probes and labeled compounds for biochem

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer therapy. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing biologically active molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to build complex heterocyclic systems. Also utilized in the preparation of fluorescent probes and labeled compounds for biochemical assays due to the presence of the iodine atom, which facilitates radiolabeling or serves as a handle for further derivatization.

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