1. Home
  2. 3-Pentyn-2-one

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

3-Pentyn-2-one

CC#CC(=O)C Request for Quotation
Chemical Name: 3-Pentyn-2-one
CAS Number: 7299-55-0
Product Number: AG008QT0(AGN-PC-0JMQH1)
Synonyms:
MDL No:
Molecular Formula: C5H6O
Molecular Weight: 82.1005

Identification/Properties

Safety Information

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Pent-3-yn-2-one is a versatile chemical compound widely used in organic synthesis for its unique properties and reactivity. As an alkyne functional group, Pent-3-yn-2-one serves as a valuable building block in the construction of various complex organic molecules. Its terminal alkyne group allows for efficient transformations through reactions such as nucleophilic addition, cycloaddition, and Sonogashira coupling. This enables the incorporation of the Pent-3-yn-2-one moiety into diverse chemical scaffolds, making it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and materials science. Additionally, the presence of the ketone group in Pent-3-yn-2-one further expands its synthetic utility, enabling selective functionalization and the formation of a wide range of functionalized derivatives. By leveraging the reactivity of Pent-3-yn-2-one, chemists can access a myriad of synthetic pathways to tailor molecules with specific functionalities and properties.