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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)-

2-(2-methoxyethyl)pyrrolidine

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Chemical Name: 2-(2-methoxyethyl)pyrrolidine
CAS Number: 933746-73-7
Product Number: AG00IHL5(AGN-PC-09ZZ3R)
Synonyms:
MDL No:
Molecular Formula: C7H15NO
Molecular Weight: 129.2001

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(2-Methoxyethyl)pyrrolidine is a versatile compound commonly utilized in chemical synthesis due to its unique properties. It serves as an efficient building block in the creation of various complex organic molecules, playing a crucial role in the development of pharmaceuticals, agrochemicals, and materials science. With its specific structural characteristics, this compound facilitates the formation of intricate chemical structures by participating in key reactions such as nucleophilic substitutions, ring closures, and asymmetric syntheses. Its ability to functionalize diverse molecular frameworks makes it a valuable tool for organic chemists striving to design novel compounds with desired properties for a wide range of applications.