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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, 1-[(methylamino)acetyl]-

CNCC(=O)N1CCCC1 Request for Quotation
Chemical Name: Pyrrolidine, 1-[(methylamino)acetyl]-
CAS Number: 144685-61-0
Product Number: AG00AB6M(AGN-PC-0LWTO7)
Synonyms:
MDL No:
Molecular Formula: C7H14N2O
Molecular Weight: 142.1989

Identification/Properties

Computed Properties
Molecular Weight:
142.202g/mol
XLogP3:
-0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
142.111g/mol
Monoisotopic Mass:
142.111g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
119
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


2-(Methylamino)-1-(pyrrolidin-1-yl)ethanone, also known as $name$, is a versatile compound frequently utilized in chemical synthesis processes. This compound serves as a crucial intermediate in the production of various pharmaceuticals, agrochemicals, and materials due to its unique chemical properties. In chemical synthesis, $name$ plays a key role as a building block for creating complex organic molecules with specific biological activities or functional properties. Its structural features make it an essential component in the development of new drug candidates, as it can be tailored to introduce specific functionalities or enhance the bioavailability of the final product. Additionally, the reactivity of $name$ allows for the formation of diverse bond types, enabling chemists to construct intricate molecular architectures efficiently. Furthermore, the presence of both amino and pyrrolidine moieties in $name$ offers opportunities for stereochemical control in the synthesis of chiral compounds, making it a valuable tool in asymmetric synthesis strategies. Overall, the application of 2-(Methylamino)-1-(pyrrolidin-1-yl)ethanone in chemical synthesis showcases its significance in advancing research and development efforts across various industries.