1-Cyclopropyl-2,6-dimethylpiperazine dihydrochloride

95%

Reagent Code: #129950
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CAS Number 1338435-11-2

science Other reagents with same CAS 1338435-11-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.17 g/mol
Formula C₉H₂₀Cl₂N₂
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves as a building block in the production of certain antimicrobial and antiviral agents due to its structural features that support bioactivity. Its piperazine core with substituted cyclopropyl and methyl groups enhances binding affinity to specific biological targets, making it valuable in medicinal chemistry research. Also employed in the preparation of novel derivatives for structure-activity relationship (SAR) studies during drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,390.00
inventory 250mg
10-20 days ฿29,560.00

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1-Cyclopropyl-2,6-dimethylpiperazine dihydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves as a building block in the production of certain antimicrobial and antiviral agents due to its structural features that support bioactivity. Its piperazine core with substituted cyclopropyl and methyl groups enhances binding affinity to specific biological targets, making it valuable in medicinal chemistry researc

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) with central nervous system activity. It serves as a building block in the production of certain antimicrobial and antiviral agents due to its structural features that support bioactivity. Its piperazine core with substituted cyclopropyl and methyl groups enhances binding affinity to specific biological targets, making it valuable in medicinal chemistry research. Also employed in the preparation of novel derivatives for structure-activity relationship (SAR) studies during drug discovery.

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