(E)-1-Bromo-4-(2-nitrovinyl)benzene

≥95%

Reagent Code: #184093
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CAS Number 5153-71-9

science Other reagents with same CAS 5153-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.04 g/mol
Formula C₈H₆BrNO₂
badge Registry Numbers
MDL Number MFCD00191856
thermostat Physical Properties
Melting Point 148-150 °C(lit.)
Boiling Point 318.9±17.0 °C
inventory_2 Storage & Handling
Density 1.596±0.06 g/cm3
Storage 2-8°C, inert gas, sealed

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of nitro-stilbene derivatives which exhibit nonlinear optical properties. It serves as a building block in the development of conjugated systems for electronic materials and fluorescent dyes. Also employed in cross-coupling reactions to form complex aromatic structures for pharmaceuticals and agrochemicals. Its vinyl bromide functionality allows for palladium-catalyzed transformations, making it valuable in medicinal chemistry research.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿580.00
1g
10-20 days ฿1,520.00
(E)-1-Bromo-4-(2-nitrovinyl)benzene
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Used as an intermediate in organic synthesis, particularly in the preparation of nitro-stilbene derivatives which exhibit nonlinear optical properties. It serves as a building block in the development of conjugated systems for electronic materials and fluorescent dyes. Also employed in cross-coupling reactions to form complex aromatic structures for pharmaceuticals and agrochemicals. Its vinyl bromide functionality allows for palladium-catalyzed transformations, making it valuable in medicinal chemistry

Used as an intermediate in organic synthesis, particularly in the preparation of nitro-stilbene derivatives which exhibit nonlinear optical properties. It serves as a building block in the development of conjugated systems for electronic materials and fluorescent dyes. Also employed in cross-coupling reactions to form complex aromatic structures for pharmaceuticals and agrochemicals. Its vinyl bromide functionality allows for palladium-catalyzed transformations, making it valuable in medicinal chemistry research.

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