3,6-Dibromo-4,5-difluorobenzene-1,2-diamine

95%

Reagent Code: #176507
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CAS Number 1345627-73-7

science Other reagents with same CAS 1345627-73-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.91 g/mol
Formula C₆H₄Br₂F₂N₂
thermostat Physical Properties
Boiling Point 327.4±37.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and brominated aromatic compounds. Its functional groups enable selective coupling reactions, making it valuable in building complex organic molecules. Commonly employed in medicinal chemistry for constructing heterocyclic systems and bioactive scaffolds. Also utilized in materials science for designing organic semiconductors and fluorescent dyes due to its electron-rich aromatic core and halogen substitution pattern.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,080.00
250mg
10-20 days ฿1,780.00
1g
10-20 days ฿5,060.00
5g
10-20 days ฿22,280.00
3,6-Dibromo-4,5-difluorobenzene-1,2-diamine
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and brominated aromatic compounds. Its functional groups enable selective coupling reactions, making it valuable in building complex organic molecules. Commonly employed in medicinal chemistry for constructing heterocyclic systems and bioactive scaffolds. Also utilized in materials science for designing organic semiconductors and fluorescent dyes due to its electron-rich aromat

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated and brominated aromatic compounds. Its functional groups enable selective coupling reactions, making it valuable in building complex organic molecules. Commonly employed in medicinal chemistry for constructing heterocyclic systems and bioactive scaffolds. Also utilized in materials science for designing organic semiconductors and fluorescent dyes due to its electron-rich aromatic core and halogen substitution pattern.

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