6-Benzyl-2-Chloro-4-Methyl-5,6,7,8-Tetrahydro-1,6-Naphthyridine

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Reagent Code: #155729
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CAS Number 1421309-97-8

science Other reagents with same CAS 1421309-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.77 g/mol
Formula C₁₆H₁₇ClN₂
badge Registry Numbers
MDL Number MFCD27997375
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly those targeting central nervous system disorders. Its structure supports the development of novel agents with potential anticonvulsant and neuroprotective properties. Also investigated for its role in kinase inhibition, making it relevant in oncology drug discovery. The compound's lipophilic nature enhances blood-brain barrier penetration, which is advantageous for CNS-targeted therapeutics.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,600.00
inventory 250mg
10-20 days ฿20,370.00
inventory 1g
10-20 days ฿66,030.00

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6-Benzyl-2-Chloro-4-Methyl-5,6,7,8-Tetrahydro-1,6-Naphthyridine
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Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly those targeting central nervous system disorders. Its structure supports the development of novel agents with potential anticonvulsant and neuroprotective properties. Also investigated for its role in kinase inhibition, making it relevant in oncology drug discovery. The compound's lipophilic nature enhances blood-brain barrier penetration, which is advantageous for CNS-targeted

Used primarily in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly those targeting central nervous system disorders. Its structure supports the development of novel agents with potential anticonvulsant and neuroprotective properties. Also investigated for its role in kinase inhibition, making it relevant in oncology drug discovery. The compound's lipophilic nature enhances blood-brain barrier penetration, which is advantageous for CNS-targeted therapeutics.

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