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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Propanenitrile, 3-(ethylamino)-

CCNCCC#N Request for Quotation
Chemical Name: Propanenitrile, 3-(ethylamino)-
CAS Number: 21539-47-9
Product Number: AG003I84(AGN-PC-0JOKVN)
Synonyms:
MDL No:
Molecular Formula: C5H10N2
Molecular Weight: 98.1463

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
98.149g/mol
XLogP3:
-0.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
98.084g/mol
Monoisotopic Mass:
98.084g/mol
Topological Polar Surface Area:
35.8A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
69.4
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

GHS Pictogram:
Signal Word:
Danger
UN#:
3267
Hazard Statements:
H302-H312-H314-H332
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Ethylamino)propanenitrile, also known as ethylamine propionitrile, serves as a versatile building block in chemical synthesis. This compound is commonly used as a key intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals.One of the primary applications of 3-(Ethylamino)propanenitrile is in the synthesis of heterocyclic compounds. By reacting with different reagents and functional groups, this compound can be transformed into a wide range of heterocycles with diverse structures and properties. These heterocycles play a vital role in the development of new drugs, pesticides, and other biologically active molecules.Furthermore, 3-(Ethylamino)propanenitrile is often utilized in the preparation of chiral compounds. Through asymmetric synthesis methods, this compound can be incorporated into enantiomerically pure molecules, which are crucial in the pharmaceutical industry for enhancing the efficacy and reducing the side effects of drugs.In addition, the presence of the ethylamino group in 3-(Ethylamino)propanenitrile allows for further functionalization reactions, enabling chemists to modify the compound for specific applications. By introducing different substituents or reactive groups, researchers can tailor the properties of the final products for desired purposes in organic synthesis.Overall, 3-(Ethylamino)propanenitrile is a valuable compound in chemical synthesis, offering a wide range of possibilities for the creation of complex molecules with diverse applications in various industries.