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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)-

Pyrrolidine, 2-ethyl-, (R)-

CC[C@@H]1CCCN1 Request for Quotation
Chemical Name: Pyrrolidine, 2-ethyl-, (R)-
CAS Number: 123168-37-6
Product Number: AG000K3U(AGN-PC-0O0KQI)
Synonyms:
MDL No:
Molecular Formula: C6H13N
Molecular Weight: 99.1741

Identification/Properties

Computed Properties
Molecular Weight:
99.177g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
99.105g/mol
Monoisotopic Mass:
99.105g/mol
Topological Polar Surface Area:
12A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
52.1
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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


(R)-2-Ethylpyrrolidine is a versatile compound widely used in chemical synthesis as a chiral building block. Its unique stereochemistry, with the ethyl group positioned at the 2-position of the pyrrolidine ring, allows for specific asymmetric transformations in organic reactions. 
This compound is especially valuable in drug synthesis, where stereochemistry plays a crucial role in determining the biological activity and pharmacological properties of the final compound. In asymmetric synthesis, (R)-2-Ethylpyrrolidine can serve as a key starting material for the construction of complex molecules with high stereoselectivity. Its use in various transformations such as asymmetric hydrogenation, addition reactions, and ring-closing processes has been well-documented in the literature. 
Overall, (R)-2-Ethylpyrrolidine is an essential tool for chemists seeking to access enantiopure compounds in a controlled and efficient manner.