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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-Cyclopropylpiperidine-2,4-dione

O=C1CCN(C(=O)C1)C1CC1 Request for Quotation
Chemical Name: 1-Cyclopropylpiperidine-2,4-dione
CAS Number: 1501330-86-4
Product Number: AG001MD1(AGN-PC-0WAFSE)
Synonyms:
MDL No:
Molecular Formula: C8H11NO2
Molecular Weight: 153.1784

Identification/Properties

Properties
Storage:
2-8℃;

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319
Precautionary Statements:
P261-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Cyclopropylpiperidine-2,4-dione is a versatile compound commonly utilized in chemical synthesis for its unique reactivity and structural properties. This compound serves as a valuable building block in the preparation of various nitrogen-containing molecules, particularly in the pharmaceutical and agrochemical industries. Due to the presence of both a piperidine ring and a cyclic ketone functionality, 1-Cyclopropylpiperidine-2,4-dione can undergo a range of regioselective transformations, including cyclization reactions, nucleophilic additions, and oxidative processes. These synthetic routes enable the incorporation of the cyclopropylpiperidine core into complex molecular frameworks, allowing for the generation of diverse bioactive compounds and intermediates. Additionally, the strained cyclopropyl group in 1-Cyclopropylpiperidine-2,4-dione imparts unique steric effects that can influence the stereochemistry and reactivity of subsequent chemical reactions, making it a valuable tool for the design and synthesis of novel molecules with specific biological activities.