Isoquinoline-4-carbonitrile

≥95%

Reagent Code: #199508
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CAS Number 34846-65-6

science Other reagents with same CAS 34846-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.17 g/mol
Formula C₁₀H₆N₂
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MDL Number MFCD00957039
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as an intermediate for bioactive compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its nitrile group allows for functional group transformations, enabling the creation of amides, amines, and heterocyclic derivatives. Employed in research settings to construct nitrogen-containing fused ring systems with potential neurological and oncological activity. Also applied in the design of fluorescent probes due to its aromatic structure and electron-withdrawing properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿980.00
5g
10-20 days ฿4,850.00
10g
10-20 days ฿9,660.00
25g
10-20 days ฿23,300.00
Isoquinoline-4-carbonitrile
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Used in pharmaceutical synthesis as an intermediate for bioactive compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its nitrile group allows for functional group transformations, enabling the creation of amides, amines, and heterocyclic derivatives. Employed in research settings to construct nitrogen-containing fused ring systems with potential neurological and oncological activity. Also applied in the design of fluorescent probes due to its aromatic structure and

Used in pharmaceutical synthesis as an intermediate for bioactive compounds, particularly in the development of kinase inhibitors and antimicrobial agents. Its nitrile group allows for functional group transformations, enabling the creation of amides, amines, and heterocyclic derivatives. Employed in research settings to construct nitrogen-containing fused ring systems with potential neurological and oncological activity. Also applied in the design of fluorescent probes due to its aromatic structure and electron-withdrawing properties.

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