(2S,5S)-5-Benzyl-3,6-dioxo-2-piperazineacetic Acid

98%

Reagent Code: #235767
label
Alias 5-benzyl-3,6-dioxo-2-piperazine acetate
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CAS Number 5262-10-2

science Other reagents with same CAS 5262-10-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.26 g/mol
Formula C₁₃H₁₄N₂O₄
badge Registry Numbers
MDL Number MFCD00190764
thermostat Physical Properties
Melting Point 270-272 °C (lit.)
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used in pharmaceutical research as a chiral building block for synthesizing peptide-based drugs. Its rigid piperazine backbone and functional groups make it suitable for developing enzyme inhibitors, particularly in neurology and oncology. The compound’s stereochemistry allows selective interaction with biological targets, enhancing drug specificity. Also explored in the design of protease inhibitors due to its ability to mimic dipeptide motifs. Its carboxylic acid and diketopiperazine groups support conjugation and improve pharmacokinetic properties in drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,680.00
inventory 1g
10-20 days ฿31,200.00
inventory 5g
10-20 days ฿113,650.00
inventory 250mg
10-20 days ฿12,600.00

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(2S,5S)-5-Benzyl-3,6-dioxo-2-piperazineacetic Acid
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Used in pharmaceutical research as a chiral building block for synthesizing peptide-based drugs. Its rigid piperazine backbone and functional groups make it suitable for developing enzyme inhibitors, particularly in neurology and oncology. The compound’s stereochemistry allows selective interaction with biological targets, enhancing drug specificity. Also explored in the design of protease inhibitors due to its ability to mimic dipeptide motifs. Its carboxylic acid and diketopiperazine groups support con

Used in pharmaceutical research as a chiral building block for synthesizing peptide-based drugs. Its rigid piperazine backbone and functional groups make it suitable for developing enzyme inhibitors, particularly in neurology and oncology. The compound’s stereochemistry allows selective interaction with biological targets, enhancing drug specificity. Also explored in the design of protease inhibitors due to its ability to mimic dipeptide motifs. Its carboxylic acid and diketopiperazine groups support conjugation and improve pharmacokinetic properties in drug candidates.

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