3-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-propylpropanamide

95%

Reagent Code: #178114
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CAS Number 1247521-37-4

science Other reagents with same CAS 1247521-37-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.23 g/mol
Formula C₁₀H₁₄N₂O₃
badge Registry Numbers
MDL Number MFCD16130341
thermostat Physical Properties
Boiling Point 433.2±28.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports conjugation in peptide-like frameworks, making it valuable in medicinal chemistry for designing protease inhibitors and targeted therapies. Also employed in the preparation of functionalized polymers and biomaterials due to its ability to participate in controlled cross-linking reactions. Commonly utilized in research settings for labeling and bioconjugation techniques, especially where selective modification of biomolecules is required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,450.00
inventory 250mg
10-20 days ฿4,050.00
inventory 1g
10-20 days ฿13,060.00

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3-(2,5-Dioxo-2,5-dihydro-1H-pyrrol-1-yl)-N-propylpropanamide
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports conjugation in peptide-like frameworks, making it valuable in medicinal chemistry for designing protease inhibitors and targeted therapies. Also employed in the preparation of functionalized polymers and biomaterials due to its ability to participate in controlled cross-linking reactions. Commonly utilized in research settings for labeling and

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports conjugation in peptide-like frameworks, making it valuable in medicinal chemistry for designing protease inhibitors and targeted therapies. Also employed in the preparation of functionalized polymers and biomaterials due to its ability to participate in controlled cross-linking reactions. Commonly utilized in research settings for labeling and bioconjugation techniques, especially where selective modification of biomolecules is required.

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