(R)-1,3-Dimethylpiperazin-2-one

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Reagent Code: #231200
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CAS Number 1240300-33-7

science Other reagents with same CAS 1240300-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.17 g/mol
Formula C₆H₁₂N₂O
badge Registry Numbers
MDL Number MFCD22201139
thermostat Physical Properties
Boiling Point 243.3±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.985±0.06 g/cm3(Predicted)
Storage Room temperature, avoid light

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure supports the formation of complex molecules with high enantioselectivity. Commonly employed in the preparation of neuroactive compounds and kinase inhibitors due to its ability to mimic peptide motifs and enhance metabolic stability. Also utilized in agrochemicals for the synthesis of bioactive molecules requiring specific stereochemical configuration.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,260.00
inventory 250mg
10-20 days ฿10,640.00
inventory 1g
10-20 days ฿34,190.00

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(R)-1,3-Dimethylpiperazin-2-one
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure supports the formation of complex molecules with high enantioselectivity. Commonly employed in the preparation of neuroactive compounds and kinase inhibitors due to its ability to mimic peptide motifs and enhance metabolic stability. Also utilized in agrochemicals for the synthesis of bioa

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure supports the formation of complex molecules with high enantioselectivity. Commonly employed in the preparation of neuroactive compounds and kinase inhibitors due to its ability to mimic peptide motifs and enhance metabolic stability. Also utilized in agrochemicals for the synthesis of bioactive molecules requiring specific stereochemical configuration.

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