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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, 3-(4-fluorophenyl)-

Fc1ccc(cc1)c1c[nH]c2c1cccc2 Request for Quotation
Chemical Name: 1H-Indole, 3-(4-fluorophenyl)-
CAS Number: 101125-32-0
Product Number: AG0003T2(AGN-PC-00MLSA)
Synonyms:
MDL No:
Molecular Formula: C14H10FN
Molecular Weight: 211.2343

Identification/Properties

Properties
MP:
102-104°C
BP:
390.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
211.239g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
211.08g/mol
Monoisotopic Mass:
211.08g/mol
Topological Polar Surface Area:
15.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
235
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H317
Precautionary Statements:
P280
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 3-(4-Fluorophenyl)-1H-indole serves as a versatile building block for creating a wide range of complex organic compounds. Due to its unique structure and reactivity, this compound is commonly used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and various fine chemicals. With its fluorophenyl group providing a useful handle for further functionalization, 3-(4-Fluorophenyl)-1H-indole allows chemists to easily introduce additional substituents or modifications to tailor the properties of the final product. Its presence in the molecular structure often imparts desirable characteristics such as enhanced bioactivity, improved stability, or specific binding properties. Through strategic manipulation and transformation, chemists can leverage the synthetic accessibility of this compound to access novel derivatives with diverse applications in medicinal chemistry, materials science, and beyond.