2-Chloro-5-Iodobenzoyl chloride

95%

Reagent Code: #164046
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CAS Number 281652-58-2

science Other reagents with same CAS 281652-58-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.91 g/mol
Formula C₇H₃Cl₂IO
badge Registry Numbers
MDL Number MFCD02628389
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive acyl chloride group allows for easy formation of amide and ester derivatives, making it valuable in constructing complex organic molecules. Commonly employed in the development of herbicides and fungicides due to the presence of halogen atoms that can enhance biological activity. Also utilized in the preparation of dyes and functional materials where halogenated aromatic structures are required. Its dual halogen functionality enables selective cross-coupling reactions, useful in fine chemical and medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,450.00
inventory 1g
10-20 days ฿6,230.00
inventory 100mg
10-20 days ฿1,590.00

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2-Chloro-5-Iodobenzoyl chloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive acyl chloride group allows for easy formation of amide and ester derivatives, making it valuable in constructing complex organic molecules. Commonly employed in the development of herbicides and fungicides due to the presence of halogen atoms that can enhance biological activity. Also utilized in the preparation of dyes and functional materials where halogenated aromatic structures are required. Its dual

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its reactive acyl chloride group allows for easy formation of amide and ester derivatives, making it valuable in constructing complex organic molecules. Commonly employed in the development of herbicides and fungicides due to the presence of halogen atoms that can enhance biological activity. Also utilized in the preparation of dyes and functional materials where halogenated aromatic structures are required. Its dual halogen functionality enables selective cross-coupling reactions, useful in fine chemical and medicinal chemistry research.

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