Methyl 1-(5-bromopyrimidin-2-yl)piperidine-4-carboxylate

98%

Reagent Code: #207093
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CAS Number 914347-01-6

science Other reagents with same CAS 914347-01-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.15 g/mol
Formula C₁₁H₁₄BrN₃O₂
badge Registry Numbers
MDL Number MFCD08275691
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 kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in drug discovery programs focused on oncology and inflammatory diseases. Commonly employed in medicinal chemistry for scaffold modification to enhance potency, metabolic stability, and bioavailability of lead compounds. Also utilized in agrochemical research for designing bioactive molecules with improved efficacy.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,760.00
inventory 5g
10-20 days ฿6,430.00
inventory 10g
10-20 days ฿12,840.00
inventory 25g
10-20 days ฿23,800.00
Methyl 1-(5-bromopyrimidin-2-yl)piperidine-4-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in drug discovery programs focused on oncology and inflammatory diseases. Commonly employed in medicinal chemistry for scaffold modification to enhance potency, metabolic stability, and bioavailability of lead compounds. Also utilized in agrochemical research for designin

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables selective binding to enzyme active sites, making it valuable in drug discovery programs focused on oncology and inflammatory diseases. Commonly employed in medicinal chemistry for scaffold modification to enhance potency, metabolic stability, and bioavailability of lead compounds. Also utilized in agrochemical research for designing bioactive molecules with improved efficacy.

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