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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)-

Methanone, 1-azetidinyl(5-chloro-2-pyrazinyl)-

O=C(c1ncc(nc1)Cl)N1CCC1 Request for Quotation
Chemical Name: Methanone, 1-azetidinyl(5-chloro-2-pyrazinyl)-
CAS Number: 915948-98-0
Product Number: AG01EBTE(AGN-PC-0801TF)
Synonyms:
MDL No:
Molecular Formula: C8H8ClN3O
Molecular Weight: 197.62162

Identification/Properties

Properties
Storage:
2-8℃;Inert atmosphere;

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


Azetidin-1-yl(5-chloropyrazin-2-yl)methanone is a versatile compound widely utilized in chemical synthesis due to its unique properties and capabilities. This compound serves as a valuable building block for the preparation of various complex organic molecules, making it an essential component in the toolbox of synthetic chemists.In chemical synthesis, Azetidin-1-yl(5-chloropyrazin-2-yl)methanone acts as a key intermediate in the construction of pharmaceuticals, agrochemicals, and materials with diverse functionalities. Its strategic incorporation into target molecules enables the introduction of important structural elements, such as azetidine and pyrazine rings, which are crucial for enhancing biological activity and physicochemical properties.Furthermore, Azetidin-1-yl(5-chloropyrazin-2-yl)methanone exhibits reactivity that allows for efficient derivatization and structural modifications, enabling chemists to tailor the properties of the final compounds for specific applications. Its ability to participate in various chemical reactions, such as nucleophilic substitution and condensation reactions, makes it an indispensable tool for the synthesis of complex molecular architectures.Overall, Azetidin-1-yl(5-chloropyrazin-2-yl)methanone plays a pivotal role in the synthesis of structurally diverse and biologically active compounds, showcasing its significance in the field of organic chemistry and drug discovery.