2-Chloro-4-methyl-5,6-dihydro-7H-cyclopenta[b]pyridin-7-one

98%

Reagent Code: #160282
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CAS Number 745075-82-5

science Other reagents with same CAS 745075-82-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.62 g/mol
Formula C₉H₈ClNO
thermostat Physical Properties
Boiling Point 355.2±42.0°C
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 central nervous system (CNS) active compounds. Its structure supports the creation of potent modulators targeting neurological receptors, making it valuable in drug discovery for conditions like epilepsy, anxiety, and neurodegenerative diseases. The compound's rigid fused ring system enhances binding selectivity and metabolic stability in final drug forms. It is also explored in the preparation of kinase inhibitors for potential oncology applications.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,480.00
inventory 250mg
10-20 days ฿13,490.00

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2-Chloro-4-methyl-5,6-dihydro-7H-cyclopenta[b]pyridin-7-one
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the creation of potent modulators targeting neurological receptors, making it valuable in drug discovery for conditions like epilepsy, anxiety, and neurodegenerative diseases. The compound's rigid fused ring system enhances binding selectivity and metabolic stability in final drug forms. It is also explored in the preparation of kin

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its structure supports the creation of potent modulators targeting neurological receptors, making it valuable in drug discovery for conditions like epilepsy, anxiety, and neurodegenerative diseases. The compound's rigid fused ring system enhances binding selectivity and metabolic stability in final drug forms. It is also explored in the preparation of kinase inhibitors for potential oncology applications.

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