2-(phenylethynyl)benzaldehyde

95%

  • Product Code: 43769
  CAS:    59046-72-9
Molecular Weight: 206.2393 g./mol Molecular Formula: C₁₅H₁₀O
EC Number: MDL Number: MFCD09030317
Melting Point: Boiling Point:
Density: 1.147g/cm3 Storage Condition: 2-8℃, dry, sealed,
Product Description: 2-(phenylethynyl)benzaldehyde is widely used in organic synthesis as a key intermediate for the preparation of various complex molecules. Its structure, featuring both an aldehyde group and a phenylethynyl moiety, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds and drug candidates. Additionally, it serves as a building block in the creation of advanced materials, such as organic semiconductors and conjugated polymers, which are essential in electronics and optoelectronics. The compound is also utilized in the synthesis of dyes and pigments due to its ability to form stable and colorful derivatives. Its versatility in cross-coupling reactions further enhances its role in constructing intricate molecular architectures for research and industrial applications.
Product Specification:
Test Specification
APPEARANCE Light-yellow to yellow Liquid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿7,890.00
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2-(phenylethynyl)benzaldehyde
2-(phenylethynyl)benzaldehyde is widely used in organic synthesis as a key intermediate for the preparation of various complex molecules. Its structure, featuring both an aldehyde group and a phenylethynyl moiety, makes it valuable in the development of pharmaceuticals, particularly in the synthesis of bioactive compounds and drug candidates. Additionally, it serves as a building block in the creation of advanced materials, such as organic semiconductors and conjugated polymers, which are essential in electronics and optoelectronics. The compound is also utilized in the synthesis of dyes and pigments due to its ability to form stable and colorful derivatives. Its versatility in cross-coupling reactions further enhances its role in constructing intricate molecular architectures for research and industrial applications.
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