Cyclopropanecarbonitrile
98%
- Product Code: 81689
Alias:
Cyclopropanenitrile; Cyclopropyl cyanide; Cyclopropylcarbonitrile
CAS:
5500-21-0
Molecular Weight: | 67.09 g./mol | Molecular Formula: | C₄H₅N |
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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 |
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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 |
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5.000 | 10-20 days | €7.91 |
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25.000 | 10-20 days | €29.81 |
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100.000 | 10-20 days | €105.53 |
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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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