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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)-

1-pyrrolidin-3-ylethanone

CC(=O)C1CNCC1 Request for Quotation
Chemical Name: 1-pyrrolidin-3-ylethanone
CAS Number: 876505-26-9
Product Number: AG00H31Y(AGN-PC-02GVVZ)
Synonyms:
MDL No:
Molecular Formula: C6H11NO
Molecular Weight: 113.1576

Identification/Properties

Computed Properties
Molecular Weight:
113.16g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
113.084g/mol
Monoisotopic Mass:
113.084g/mol
Topological Polar Surface Area:
29.1A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
101
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

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(Pyrrolidin-3-yl)ethanone, also known as pyrrolidin-3-yl ketone, is a versatile compound commonly used in chemical synthesis. Its unique structure containing both a pyrrolidine ring and a ketone functional group lends itself to a variety of applications in organic chemistry.In chemical synthesis, 1-(Pyrrolidin-3-yl)ethanone serves as a valuable building block for the preparation of various organic compounds. Its ketone group allows for facile modification through a range of chemical reactions, enabling the introduction of different functional groups or stereochemical elements into the molecule. Additionally, its pyrrolidine ring confers specific steric and electronic properties that can influence the reactivity and properties of the final product.One common application of 1-(Pyrrolidin-3-yl)ethanone is in the synthesis of pharmaceutical intermediates and bioactive compounds. By incorporating this key building block into the molecular structure, chemists can tailor the properties of the target molecule to enhance its efficacy, bioavailability, or selectivity. Furthermore, the presence of the pyrrolidine ring in the molecule can impart biological activity or mimic natural products, making it a valuable scaffold for drug discovery efforts.Overall, the versatility and unique structural features of 1-(Pyrrolidin-3-yl)ethanone make it a valuable tool in chemical synthesis, particularly in the development of novel organic compounds with potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science.