Ethyl 5-chloro-7-fluoro-1H-indole-2-carboxylate

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Reagent Code: #184650
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CAS Number 1204501-37-0

science Other reagents with same CAS 1204501-37-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.65 g/mol
Formula C₁₁H₉ClFNO₂
badge Registry Numbers
MDL Number MFCD22205716
thermostat Physical Properties
Melting Point 178-179 °C(Solv: hexane (110-54-3))
Boiling Point 372.6±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.401±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective kinase inhibitors and anti-inflammatory compounds. Its structure supports functionalization at multiple sites, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to design drugs targeting neurological disorders and certain cancers due to its ability to cross the blood-brain barrier and interact with central nervous system receptors. Also utilized in the preparation of fluorinated indole derivatives, which show enhanced metabolic stability and bioavailability in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,660.00
inventory 250mg
10-20 days ฿31,100.00

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Ethyl 5-chloro-7-fluoro-1H-indole-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective kinase inhibitors and anti-inflammatory compounds. Its structure supports functionalization at multiple sites, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to design drugs targeting neurological disorders and certain cancers due to its ability to cross the blood-brain barrier and interact with central nervous

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of selective kinase inhibitors and anti-inflammatory compounds. Its structure supports functionalization at multiple sites, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in research settings to design drugs targeting neurological disorders and certain cancers due to its ability to cross the blood-brain barrier and interact with central nervous system receptors. Also utilized in the preparation of fluorinated indole derivatives, which show enhanced metabolic stability and bioavailability in drug candidates.

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