(S)-2-Amino-5-(4-methoxy-7-nitroindolin-1-yl)-5-oxopentanoic acid

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Reagent Code: #233153
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CAS Number 295325-62-1

science Other reagents with same CAS 295325-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 323.3 g/mol
Formula C₁₄H₁₇N₃O₆
thermostat Physical Properties
Melting Point >160 °C(dec.)
Boiling Point 675.1±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.437±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in the synthesis of photoremovable protecting groups for amino acids and peptides. Enables light-controlled release of bioactive molecules in research settings, particularly in neuroscience and cell biology for precise spatiotemporal activation. Commonly applied in studies involving caged glutamate, allowing targeted stimulation of neurons with high temporal and spatial resolution. Its nitroindoline-based structure provides good photochemical stability and efficient uncaging upon exposure to near-UV light.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿15,290.00
inventory 25mg
10-20 days ฿53,240.00

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(S)-2-Amino-5-(4-methoxy-7-nitroindolin-1-yl)-5-oxopentanoic acid
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Used as a key intermediate in the synthesis of photoremovable protecting groups for amino acids and peptides. Enables light-controlled release of bioactive molecules in research settings, particularly in neuroscience and cell biology for precise spatiotemporal activation. Commonly applied in studies involving caged glutamate, allowing targeted stimulation of neurons with high temporal and spatial resolution. Its nitroindoline-based structure provides good photochemical stability and efficient uncaging up

Used as a key intermediate in the synthesis of photoremovable protecting groups for amino acids and peptides. Enables light-controlled release of bioactive molecules in research settings, particularly in neuroscience and cell biology for precise spatiotemporal activation. Commonly applied in studies involving caged glutamate, allowing targeted stimulation of neurons with high temporal and spatial resolution. Its nitroindoline-based structure provides good photochemical stability and efficient uncaging upon exposure to near-UV light.

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