5-Chloro-[1,1'-biphenyl]-2-amine

97%

Reagent Code: #161921
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CAS Number 73006-78-7

science Other reagents with same CAS 73006-78-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.67 g/mol
Formula C₁₂H₁₀ClN
badge Registry Numbers
MDL Number MFCD23713168
thermostat Physical Properties
Boiling Point 339.8°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.205g/cm3
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. It serves as a building block in organic reactions where chlorinated biphenyl scaffolds are required. Its amine group allows for further functionalization, enabling the creation of more complex molecules in drug discovery and crop protection chemistry. Also employed in research settings for designing ligands and catalysts in asymmetric synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,670.00
inventory 1g
10-20 days ฿8,010.00
inventory 250mg
10-20 days ฿2,020.00

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5-Chloro-[1,1'-biphenyl]-2-amine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. It serves as a building block in organic reactions where chlorinated biphenyl scaffolds are required. Its amine group allows for further functionalization, enabling the creation of more complex molecules in drug discovery and crop protection chemistry. Also employed in research settings for designing ligands and catalysts in asymmetric synthesis.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. It serves as a building block in organic reactions where chlorinated biphenyl scaffolds are required. Its amine group allows for further functionalization, enabling the creation of more complex molecules in drug discovery and crop protection chemistry. Also employed in research settings for designing ligands and catalysts in asymmetric synthesis.

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