5-Bromo-2-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile

95%

  • Product Code: 124389
  CAS:    876918-62-6
Molecular Weight: 282.13 g./mol Molecular Formula: C₁₂H₁₂BrNO₂
EC Number: MDL Number: MFCD22393669
Melting Point: Boiling Point: 395.5±42.0 °C at 760 mmHg
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring a bromo and cyano group, makes it a valuable building block in medicinal chemistry, particularly for designing compounds with potential therapeutic properties. It is often employed in the creation of small molecule inhibitors or modulators targeting specific biological pathways. Additionally, it may be used in organic synthesis for constructing heterocyclic compounds, which are essential in drug discovery and agrochemical applications. Its stability and reactivity also make it suitable for use in cross-coupling reactions, a key technique in modern synthetic chemistry.
Product Specification:
Test Specification
Appearance White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿3,230.00
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0.250 10-20 days ฿5,480.00
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1.000 10-20 days ฿14,770.00
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5-Bromo-2-((tetrahydro-2H-pyran-4-yl)oxy)benzonitrile
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of more complex molecules. Its structure, featuring a bromo and cyano group, makes it a valuable building block in medicinal chemistry, particularly for designing compounds with potential therapeutic properties. It is often employed in the creation of small molecule inhibitors or modulators targeting specific biological pathways. Additionally, it may be used in organic synthesis for constructing heterocyclic compounds, which are essential in drug discovery and agrochemical applications. Its stability and reactivity also make it suitable for use in cross-coupling reactions, a key technique in modern synthetic chemistry.
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