(3S)-4-Chloro-3-[(triMethylsilyl)oxy]butanenitrile

94%

  • Product Code: 80486
  CAS:    727382-14-1
Molecular Weight: 191.73 g./mol Molecular Formula: C₇H₁₄ClNOSi
EC Number: MDL Number:
Melting Point: Boiling Point: 233.8±20.0 °C(Predicted)
Density: 1.002±0.06 g/cm3(Predicted) Storage Condition: room temperature
Product Description: This chemical is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and fine chemicals. Its structure, featuring a chloro and silyloxy group, makes it a versatile building block for constructing complex molecules. It is often employed in stereoselective reactions, particularly in the synthesis of chiral compounds, due to its ability to influence the stereochemistry of the final product. Additionally, it is used in the preparation of β-amino acids and other nitrogen-containing compounds, which are essential in drug development and medicinal chemistry. Its reactivity and functional groups allow for further modifications, making it valuable in the design and synthesis of biologically active molecules.
Product Specification:
Test Specification
APPEARANCE Brown liquid
PURITY 93.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days €11.87
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25.000 10-20 days €34.03
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100.000 10-20 days €104.47
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500.000 10-20 days €284.93
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(3S)-4-Chloro-3-[(triMethylsilyl)oxy]butanenitrile
This chemical is primarily utilized in organic synthesis as a key intermediate for the production of various pharmaceuticals and fine chemicals. Its structure, featuring a chloro and silyloxy group, makes it a versatile building block for constructing complex molecules. It is often employed in stereoselective reactions, particularly in the synthesis of chiral compounds, due to its ability to influence the stereochemistry of the final product. Additionally, it is used in the preparation of β-amino acids and other nitrogen-containing compounds, which are essential in drug development and medicinal chemistry. Its reactivity and functional groups allow for further modifications, making it valuable in the design and synthesis of biologically active molecules.
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