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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)-

1H-Indole, 6-fluoro-3-(4-piperidinyl)-

Fc1ccc2c(c1)[nH]cc2C1CCNCC1 Request for Quotation
Chemical Name: 1H-Indole, 6-fluoro-3-(4-piperidinyl)-
CAS Number: 76315-55-4
Product Number: AG005E6O(AGN-PC-0NFTFY)
Synonyms:
MDL No:
Molecular Formula: C13H15FN2
Molecular Weight: 218.2700

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
218.275g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
218.122g/mol
Monoisotopic Mass:
218.122g/mol
Topological Polar Surface Area:
27.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
240
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

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


6-Fluoro-3-(piperidin-4-yl)-1H-indole, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in the development of various pharmaceuticals and agrochemicals due to its unique structural properties and reactivity.In chemical synthesis, $name$ serves as a valuable building block for the construction of complex molecules. Its fluoro-substituted indole ring provides a strategic site for further functionalization, allowing for the introduction of diverse chemical moieties. The presence of a piperidine group in close proximity offers additional opportunities for selective derivatization, enabling the synthesis of structurally diverse compounds with specific biological activities.$name$ is particularly valuable in the synthesis of heterocyclic compounds, which are prevalent in numerous bioactive molecules. By incorporating this key intermediate into synthetic pathways, chemists can efficiently access a wide range of novel compounds with potential pharmaceutical or agrochemical applications. Its well-defined structure and reactivity make $name$ a versatile tool for designing and developing new drug candidates or crop protection agents with enhanced properties.Overall, the application of 6-Fluoro-3-(piperidin-4-yl)-1H-indole in chemical synthesis enables researchers to explore innovative pathways for the creation of functional molecules with diverse biological activities. Its significance in synthetic chemistry underscores its importance as a valuable building block for the discovery and development of new compounds for various applications.