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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)-

2-fluoro-4-(4-methylpiperazin-1-yl)benzaldehyde

O=Cc1ccc(cc1F)N1CCN(CC1)C Request for Quotation
Chemical Name: 2-fluoro-4-(4-methylpiperazin-1-yl)benzaldehyde
CAS Number: 1197193-42-2
Product Number: AG000PJS(AGN-PC-09SGGE)
Synonyms:
MDL No: MFCD13191597
Molecular Formula: C12H15FN2O
Molecular Weight: 222.2587

Identification/Properties

Properties
Storage:
Room Temperature;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Fluoro-4-(4-methyl-1-piperazinyl)benzaldehyde is widely utilized in chemical synthesis as a versatile intermediate. With its unique structure combining a fluoro substituent and a piperazine ring, this compound serves as a key building block in the development of various pharmaceuticals, agrochemicals, and specialty chemicals. In organic synthesis, it participates in a variety of reactions including Mannich reactions, reductive aminations, and condensations to introduce functionality and complexity into molecules. Its strategic placement of functional groups allows for efficient modification and diversification, enabling the formation of important chemical bonds. Overall, the application of 2-Fluoro-4-(4-methyl-1-piperazinyl)benzaldehyde in chemical synthesis showcases its significance as a valuable tool for the creation of novel compounds with potential biological activities.