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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)-

3-[(2R)-1-ethylpyrrolidin-2-yl]pyridine

CCN1CCCC1c1cccnc1 Request for Quotation
Chemical Name: 3-[(2R)-1-ethylpyrrolidin-2-yl]pyridine
CAS Number: 86900-39-2
Product Number: AG004PBU(AGN-PC-05XVV1)
Synonyms:
MDL No:
Molecular Formula: C11H16N2
Molecular Weight: 176.2581

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
176.263g/mol
XLogP3:
1.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
176.131g/mol
Monoisotopic Mass:
176.131g/mol
Topological Polar Surface Area:
16.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
158
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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-(1-Ethylpyrrolidin-2-yl)pyridine, also known as $name$, is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. In organic synthesis, this compound serves as a valuable building block for the preparation of various pharmaceuticals, agrochemicals, and functional materials.One primary application of 3-(1-Ethylpyrrolidin-2-yl)pyridine is as a ligand in transition metal-catalyzed reactions. Its nitrogen-containing heterocyclic structure allows for strong coordination with metal ions, enabling efficient catalysis in a wide range of chemical transformations. This compound has been employed in cross-coupling reactions, C-H activation, and asymmetric catalysis, facilitating the formation of complex organic molecules with high selectivity and efficiency.Furthermore, 3-(1-Ethylpyrrolidin-2-yl)pyridine plays a crucial role in the synthesis of biologically active compounds. By serving as a key intermediate in the construction of pharmacologically relevant molecules, it contributes to the development of new drugs and therapeutic agents. Its structural versatility and stability make it an essential component in the design and optimization of novel synthetic routes for drug discovery and development.Overall, the application of 3-(1-Ethylpyrrolidin-2-yl)pyridine in chemical synthesis highlights its significance as a valuable tool for creating diverse compounds with potential applications in various scientific and industrial fields.