(E)-4-(Piperidin-1-yl)but-2-enoic acid hydrochloride

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Reagent Code: #183646
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CAS Number 197892-69-6

science Other reagents with same CAS 197892-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.68 g/mol
Formula C₉H₁₆ClNO₂
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MDL Number MFCD14636476
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for conjugation into larger molecules where modulation of enzyme activity is required. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory and oncological pathways. The hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction environments and biological assays.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,100.00
inventory 10g
10-20 days ฿1,970.00
inventory 25g
10-20 days ฿4,190.00
inventory 100g
10-20 days ฿14,540.00
inventory 500g
10-20 days ฿46,970.00

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(E)-4-(Piperidin-1-yl)but-2-enoic acid hydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for conjugation into larger molecules where modulation of enzyme activity is required. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory and oncological pathways. The hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction environments and

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for conjugation into larger molecules where modulation of enzyme activity is required. Commonly employed in medicinal chemistry for optimizing drug candidates targeting inflammatory and oncological pathways. The hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction environments and biological assays.

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