Cyclopropanecarbonitrile

98%

  • Product Code: 81689
  Alias:    Cyclopropanenitrile; Cyclopropyl cyanide; Cyclopropylcarbonitrile
  CAS:    5500-21-0
Molecular Weight: 67.09 g./mol Molecular Formula: C₄H₅N
EC Number: MDL Number: MFCD00001269
Melting Point: Boiling Point:
Density: 0.911 g/mL at 25 °C (lit.) Storage Condition: 2~8℃
Product Description: Cyclopropanecarbonitrile is primarily utilized in organic synthesis as a versatile building block for the construction of more complex molecules. Its strained cyclopropane ring and nitrile functional group make it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in cycloaddition reactions, where the three-membered ring can participate in ring-opening processes to form new carbon-carbon bonds. Additionally, the nitrile group can be further transformed into various functional groups, such as amines, carboxylic acids, or amides, enhancing its utility in multi-step synthetic routes. In medicinal chemistry, it serves as a precursor for the development of biologically active compounds, including potential drug candidates targeting specific enzymes or receptors. Its unique structure also makes it a subject of interest in the study of reaction mechanisms and stereochemistry.
Product Specification:
Test Specification
APPEARANCE Colorless to Red to Green clear liquid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿300.00
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-
25.000 10-20 days ฿1,130.00
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-
100.000 10-20 days ฿4,000.00
+
-
Cyclopropanecarbonitrile
Cyclopropanecarbonitrile is primarily utilized in organic synthesis as a versatile building block for the construction of more complex molecules. Its strained cyclopropane ring and nitrile functional group make it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in cycloaddition reactions, where the three-membered ring can participate in ring-opening processes to form new carbon-carbon bonds. Additionally, the nitrile group can be further transformed into various functional groups, such as amines, carboxylic acids, or amides, enhancing its utility in multi-step synthetic routes. In medicinal chemistry, it serves as a precursor for the development of biologically active compounds, including potential drug candidates targeting specific enzymes or receptors. Its unique structure also makes it a subject of interest in the study of reaction mechanisms and stereochemistry.
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