((2S,5S)-5-Methylpiperazin-2-yl)methanol dihydrochloride

95%

Reagent Code: #235982
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CAS Number 2407907-33-7

science Other reagents with same CAS 2407907-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.11 g/mol
Formula C₆H₁₆Cl₂N₂O
badge Registry Numbers
MDL Number MFCD32639266
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral piperazine scaffolds. Its functional groups enable coupling reactions in drug design, especially in central nervous system agents and antimicrobial compounds. The dihydrochloride salt form enhances stability and solubility, making it suitable for use in aqueous reaction conditions and purification processes during manufacturing. Commonly employed in research settings for structure-activity relationship (SAR) studies due to its stereochemistry and derivatization potential.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,070.00
inventory 250mg
10-20 days ฿9,760.00
inventory 1g
10-20 days ฿38,020.00
((2S,5S)-5-Methylpiperazin-2-yl)methanol dihydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral piperazine scaffolds. Its functional groups enable coupling reactions in drug design, especially in central nervous system agents and antimicrobial compounds. The dihydrochloride salt form enhances stability and solubility, making it suitable for use in aqueous reaction conditions and purification processes during manufacturing. Commonly employed in

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral piperazine scaffolds. Its functional groups enable coupling reactions in drug design, especially in central nervous system agents and antimicrobial compounds. The dihydrochloride salt form enhances stability and solubility, making it suitable for use in aqueous reaction conditions and purification processes during manufacturing. Commonly employed in research settings for structure-activity relationship (SAR) studies due to its stereochemistry and derivatization potential.

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