tert-Butyl5-chloro-3,4-dihydro-2,6-naphthyridine-2(1H)-carboxylate

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Reagent Code: #154478
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CAS Number 1196153-26-0

science Other reagents with same CAS 1196153-26-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.74 g/mol
Formula C₁₃H₁₇ClN₂O₂
badge Registry Numbers
MDL Number MFCD11977790
inventory_2 Storage & Handling
Storage 2-8°C

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 potent and targeted drug candidates. Commonly employed in medicinal chemistry research to build complex heterocyclic systems with biological activity. Also utilized in the preparation of compounds targeting central nervous system disorders due to its ability to cross the blood-brain barrier.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,180.00
inventory 250mg
10-20 days ฿10,360.00
inventory 1g
10-20 days ฿37,700.00

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tert-Butyl5-chloro-3,4-dihydro-2,6-naphthyridine-2(1H)-carboxylate
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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 potent and targeted drug candidates. Commonly employed in medicinal chemistry research to build complex heterocyclic systems with biological activity. Also utilized in the preparation of compounds targeting central nervous system disorders due to its ability to cross the blood-bra

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 potent and targeted drug candidates. Commonly employed in medicinal chemistry research to build complex heterocyclic systems with biological activity. Also utilized in the preparation of compounds targeting central nervous system disorders due to its ability to cross the blood-brain barrier.

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