5-Isopropylindoline-2,3-dione

95%

Reagent Code: #200248
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CAS Number 150560-58-0

science Other reagents with same CAS 150560-58-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.21 g/mol
Formula C₁₁H₁₁NO₂
badge Registry Numbers
MDL Number MFCD02947184
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Shows potential in the development of kinase inhibitors and anticancer agents due to its structural similarity to known bioactive indoline derivatives. Also employed in the preparation of dyes and functional materials where indoline-based scaffolds enhance photostability and electron-donating properties. Its keto-functional groups allow for derivatization in multi-step synthesis, making it valuable in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,220.00
inventory 250mg
10-20 days ฿1,920.00
inventory 1g
10-20 days ฿5,500.00
inventory 5g
10-20 days ฿22,720.00

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5-Isopropylindoline-2,3-dione
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Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Shows potential in the development of kinase inhibitors and anticancer agents due to its structural similarity to known bioactive indoline derivatives. Also employed in the preparation of dyes and functional materials where indoline-based scaffolds enhance photostability and electron-donating properties. Its keto-functional groups allow for derivatization in multi-step synthesis, making it valuable in medi

Used in organic synthesis as an intermediate for pharmaceuticals and biologically active compounds. Shows potential in the development of kinase inhibitors and anticancer agents due to its structural similarity to known bioactive indoline derivatives. Also employed in the preparation of dyes and functional materials where indoline-based scaffolds enhance photostability and electron-donating properties. Its keto-functional groups allow for derivatization in multi-step synthesis, making it valuable in medicinal chemistry research.

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