Propanenitrile, 3-(cyclopropylamino)-


Chemical Name: Propanenitrile, 3-(cyclopropylamino)-
CAS Number: 58196-47-7
Product Number: AG003I2B(AGN-PC-0JMTBT)
Synonyms:
MDL No:
Molecular Formula: C6H10N2
Molecular Weight: 110.1570

Identification/Properties


Properties
Storage:
Room Temperature;Light sensitive;Inert atmosphere;
Computed Properties
Molecular Weight:
110.16g/mol
XLogP3:
0.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
110.084g/mol
Monoisotopic Mass:
110.084g/mol
Topological Polar Surface Area:
35.8A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
107
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


NMR Spectrum


Other Analytical Data


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Chemical Structure



3-(Cyclopropylamino)propionitrile, often referred to simply as propionitrile, is a versatile organic compound commonly used in chemical synthesis. This molecule serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. One key application of 3-(Cyclopropylamino)propionitrile is in the production of complex nitrogen-containing compounds through its ability to undergo various chemical reactions, such as nucleophilic addition and substitution reactions. Chemists utilize this compound to introduce the cyclopropylamino group into target molecules, enabling the synthesis of diverse chemical structures with unique properties and applications. In the realm of medicinal chemistry, 3-(Cyclopropylamino)propionitrile plays a crucial role in the synthesis of bioactive compounds, including potential drug candidates with enhanced pharmacological activities. Its utility extends to the creation of novel materials, catalysts, and functionalized molecules in organic synthesis, demonstrating its significance as a valuable tool in modern chemical research and development.