2-(Pent-4-yn-1-yl)isoindoline-1,3-dione

98%

Reagent Code: #224953
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CAS Number 6097-07-0

science Other reagents with same CAS 6097-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.23 g/mol
Formula C₁₃H₁₁NO₂
badge Registry Numbers
MDL Number MFCD06798110
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized heterocyclic compounds. Its alkyne functionality enables click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in pharmaceutical research and development of bioactive molecules. Commonly employed in the synthesis of fluorescent probes and labeled biomolecules due to the ease of modifying the isoindoline dione ring. Also finds use in polymer chemistry for creating cross-linked networks and functional materials through alkyne-based coupling reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿610.00
1g
10-20 days ฿1,520.00
5g
10-20 days ฿4,520.00
50g
10-20 days ฿27,580.00
2-(Pent-4-yn-1-yl)isoindoline-1,3-dione
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Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized heterocyclic compounds. Its alkyne functionality enables click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in pharmaceutical research and development of bioactive molecules. Commonly employed in the synthesis of fluorescent probes and labeled biomolecules due to the ease of modifying the isoindoline dione ring. Also finds use in polymer chemistry for

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized heterocyclic compounds. Its alkyne functionality enables click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in pharmaceutical research and development of bioactive molecules. Commonly employed in the synthesis of fluorescent probes and labeled biomolecules due to the ease of modifying the isoindoline dione ring. Also finds use in polymer chemistry for creating cross-linked networks and functional materials through alkyne-based coupling reactions.

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