4-[(Trimethylsilyl)ethynyl]pyridine

≥95%

  • Product Code: 69930
  CAS:    133810-35-2
Molecular Weight: 175.30 g./mol Molecular Formula: C₁₀H₁₃NSi
EC Number: MDL Number: MFCD09258874
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, dry
Product Description: This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is particularly valuable in the preparation of pyridine derivatives, which are important in pharmaceuticals and agrochemicals. The trimethylsilyl group acts as a protecting group for the ethynyl functionality, allowing selective reactions to occur at other sites of the molecule. Additionally, it is employed in the development of materials for organic electronics, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), due to its ability to modify electronic properties. Its ethynyl group also makes it a useful intermediate in click chemistry reactions, facilitating the creation of diverse molecular architectures.
Product Specification:
Test Specification
APPEARANCE Colorless to brown liquid
PURITY 94.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days ฿1,220.00
+
-
0.100 10-20 days ฿3,360.00
+
-
0.250 10-20 days ฿5,890.00
+
-
1.000 10-20 days ฿13,910.00
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-
4-[(Trimethylsilyl)ethynyl]pyridine
This chemical is primarily used in organic synthesis as a building block for more complex molecules. It is particularly valuable in the preparation of pyridine derivatives, which are important in pharmaceuticals and agrochemicals. The trimethylsilyl group acts as a protecting group for the ethynyl functionality, allowing selective reactions to occur at other sites of the molecule. Additionally, it is employed in the development of materials for organic electronics, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), due to its ability to modify electronic properties. Its ethynyl group also makes it a useful intermediate in click chemistry reactions, facilitating the creation of diverse molecular architectures.
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