(R)-2,2-Dimethyl-1-(3-methyl-4-(5-nitropyridin-2-yl)piperazin-1-yl)propan-1-one

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Reagent Code: #230702
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CAS Number 1956437-90-3

science Other reagents with same CAS 1956437-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.36 g/mol
Formula C₁₅H₂₂N₄O₃
badge Registry Numbers
MDL Number MFCD27924144
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to central nervous system disorders due to its ability to cross the blood-brain barrier. Also employed in the design of selective receptor modulators for treating inflammatory and neurodegenerative diseases. Its nitro-pyridine moiety contributes to strong binding interactions in enzyme inhibition assays, making it valuable in early-stage drug discovery.

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inventory 1g
10-20 days ฿35,480.00

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(R)-2,2-Dimethyl-1-(3-methyl-4-(5-nitropyridin-2-yl)piperazin-1-yl)propan-1-one
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to central nervous system disorders due to its ability to cross the blood-brain barrier. Also employed in the design of selective receptor modulators for treating inflammatory and neurodegenerative diseases. Its nitro-pyridine moiety contributes to strong binding interactions in enzyme inhibition assays, making it

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to central nervous system disorders due to its ability to cross the blood-brain barrier. Also employed in the design of selective receptor modulators for treating inflammatory and neurodegenerative diseases. Its nitro-pyridine moiety contributes to strong binding interactions in enzyme inhibition assays, making it valuable in early-stage drug discovery.

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