(3-Amino-piperidin-1-yl)-pyrazin-2-yl-methanonehydrochloride

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Reagent Code: #138224
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CAS Number 1185316-35-1

science Other reagents with same CAS 1185316-35-1

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scatter_plot Molecular Information
Weight 242.705 g/mol
Formula C₁₀H₁₅ClN₄O
badge Registry Numbers
MDL Number MFCD09607874
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Commonly employed in research for central nervous system drugs due to its ability to cross the blood-brain barrier. Also utilized in the preparation of bioactive molecules with antimicrobial and anti-inflammatory properties. Valued in medicinal chemistry for its role in improving metabolic stability and solubility of drug candidates.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿32,600.00

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(3-Amino-piperidin-1-yl)-pyrazin-2-yl-methanonehydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Commonly employed in research for central nervous system drugs due to its ability to cross the blood-brain barrier. Also utilized in the preparation of bioactive molecules with antimicrobial and anti-inflammatory properties. Valued in medicinal chemistry for its role in imp

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for cancer treatment. Its structure supports binding to enzyme active sites, enhancing selectivity and potency. Commonly employed in research for central nervous system drugs due to its ability to cross the blood-brain barrier. Also utilized in the preparation of bioactive molecules with antimicrobial and anti-inflammatory properties. Valued in medicinal chemistry for its role in improving metabolic stability and solubility of drug candidates.

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