5,7-Dichloro-3-Methylthieno[3,2-b]Pyridine

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Reagent Code: #178894
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CAS Number 952435-06-2

science Other reagents with same CAS 952435-06-2

blur_circular Chemical Specifications

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Weight 218.1 g/mol
Formula C₈H₅Cl₂NS
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the design of molecules with high selectivity toward specific enzyme receptors. It is also employed in research settings to explore new heterocyclic compounds with potential biological activity. The compound's halogen and methyl group positioning enhances reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug-like molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,280.00
inventory 250mg
10-20 days ฿12,530.00
inventory 500mg
10-20 days ฿20,850.00
inventory 1g
10-20 days ฿34,770.00

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5,7-Dichloro-3-Methylthieno[3,2-b]Pyridine
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the design of molecules with high selectivity toward specific enzyme receptors. It is also employed in research settings to explore new heterocyclic compounds with potential biological activity. The compound's halogen and methyl group positioning enhances reactivity in cross-coupling reactions, making it valuable in medicinal chem

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports the design of molecules with high selectivity toward specific enzyme receptors. It is also employed in research settings to explore new heterocyclic compounds with potential biological activity. The compound's halogen and methyl group positioning enhances reactivity in cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug-like molecules.

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