Benzoic acid, 4-(5-bromo-2-pyridinyl)-

95%

Reagent Code: #141747
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CAS Number 1255635-99-4

science Other reagents with same CAS 1255635-99-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.1014 g/mol
Formula C₁₂H₈BrNO₂
badge Registry Numbers
MDL Number MFCD17677961
thermostat Physical Properties
Boiling Point 419.6±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.574±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to bind effectively with biological targets through hydrogen bonding and aromatic interactions. Also employed in research settings for the preparation of pyridine-based derivatives with potential anti-inflammatory and antimicrobial activities. Its bromine functionality allows for further chemical modifications via cross-coupling reactions, making it valuable in drug discovery and development.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,200.00
inventory 250mg
10-20 days ฿30,400.00
inventory 1g
10-20 days ฿60,800.00

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Benzoic acid, 4-(5-bromo-2-pyridinyl)-
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to bind effectively with biological targets through hydrogen bonding and aromatic interactions. Also employed in research settings for the preparation of pyridine-based derivatives with potential anti-inflammatory and antimicrobial activities. Its bromine functionality allows for further che

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to bind effectively with biological targets through hydrogen bonding and aromatic interactions. Also employed in research settings for the preparation of pyridine-based derivatives with potential anti-inflammatory and antimicrobial activities. Its bromine functionality allows for further chemical modifications via cross-coupling reactions, making it valuable in drug discovery and development.

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