5-chloro-1,3-benzodioxole-4-carboxaldehyde

98%

Reagent Code: #157438
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CAS Number 249636-63-3

science Other reagents with same CAS 249636-63-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.58 g/mol
Formula C₈H₅ClO₃
badge Registry Numbers
MDL Number MFCD24684054
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, antibacterial, or insecticidal properties. Its aldehyde functional group allows for easy modification in organic reactions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in condensation reactions to form Schiff bases or in the preparation of dyes and fluorescent probes due to its aromatic and electron-rich structure.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿7,630.00
250mg
10-20 days ฿11,710.00
1g
10-20 days ฿23,790.00
5-chloro-1,3-benzodioxole-4-carboxaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, antibacterial, or insecticidal properties. Its aldehyde functional group allows for easy modification in organic reactions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in condensation reactions to form Schiff bases or in the preparation of dyes and fluorescent probes due to its aromatic and electron-rich structure.<

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, antibacterial, or insecticidal properties. Its aldehyde functional group allows for easy modification in organic reactions, making it valuable in constructing complex heterocyclic compounds. Commonly employed in condensation reactions to form Schiff bases or in the preparation of dyes and fluorescent probes due to its aromatic and electron-rich structure.

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