7-Chloro-3-iodo-1H-pyrrolo[3,2-b]pyridine

≥95%

Reagent Code: #161888
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CAS Number 1190318-10-5

science Other reagents with same CAS 1190318-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.48 g/mol
Formula C₇H₄ClIN₂
badge Registry Numbers
MDL Number MFCD12963113
thermostat Physical Properties
Boiling Point 374.0±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating targeted therapies. It is also employed in the preparation of bioactive molecules in medicinal chemistry research, where the presence of both chlorine and iodine enables further functionalization through cross-coupling reactions. Commonly utilized in the formation of potential antitumor and antiviral agents due to its heterocyclic framework and reactivity profile.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,040.00
inventory 250mg
10-20 days ฿4,690.00

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7-Chloro-3-iodo-1H-pyrrolo[3,2-b]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating targeted therapies. It is also employed in the preparation of bioactive molecules in medicinal chemistry research, where the presence of both chlorine and iodine enables further functionalization through cross-coupling reactions. Commonly utilized in the formation of potential ant

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating targeted therapies. It is also employed in the preparation of bioactive molecules in medicinal chemistry research, where the presence of both chlorine and iodine enables further functionalization through cross-coupling reactions. Commonly utilized in the formation of potential antitumor and antiviral agents due to its heterocyclic framework and reactivity profile.

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