6'-METHOXYSPIRO[CYCLOPROPANE-1,3'-INDOLINE]

95%

Reagent Code: #66074
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CAS Number 1523068-91-8

science Other reagents with same CAS 1523068-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175 g/mol
Formula C₁₁H₁₃NO
badge Registry Numbers
MDL Number MFCD27922331
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its unique structure, featuring a spirocyclopropane and indoline moiety, makes it a valuable intermediate in the creation of biologically active molecules. Researchers often explore its potential in designing compounds with therapeutic properties, such as anti-inflammatory, anticancer, or neuroprotective effects. Additionally, its methoxy group enhances its reactivity and solubility, facilitating its incorporation into complex chemical frameworks during drug discovery processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿240,300.00
inventory 250mg
10-20 days ฿91,260.00

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6'-METHOXYSPIRO[CYCLOPROPANE-1,3'-INDOLINE]
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its unique structure, featuring a spirocyclopropane and indoline moiety, makes it a valuable intermediate in the creation of biologically active molecules. Researchers often explore its potential in designing compounds with therapeutic properties, such as anti-inflammatory, anticancer, or neuroprotective effects. Additionally, its methoxy group enhances its reactivity an

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its unique structure, featuring a spirocyclopropane and indoline moiety, makes it a valuable intermediate in the creation of biologically active molecules. Researchers often explore its potential in designing compounds with therapeutic properties, such as anti-inflammatory, anticancer, or neuroprotective effects. Additionally, its methoxy group enhances its reactivity and solubility, facilitating its incorporation into complex chemical frameworks during drug discovery processes.

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