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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, 2-(4-bromophenyl)-

Brc1ccc(cc1)c1cc2c([nH]1)cccc2 Request for Quotation
Chemical Name: 1H-Indole, 2-(4-bromophenyl)-
CAS Number: 6127-49-7
Product Number: AG00E9T9(AGN-PC-0JTYU3)
Synonyms:
MDL No:
Molecular Formula: C14H10BrN
Molecular Weight: 272.1399

Identification/Properties

Computed Properties
Molecular Weight:
272.145g/mol
XLogP3:
4.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
1
Exact Mass:
271g/mol
Monoisotopic Mass:
271g/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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(4-Bromophenyl)-1H-indole is a versatile compound widely utilized in chemical synthesis for its unique properties and reactivity. Known for its substituted phenyl group and indole ring structure, this molecule serves as a valuable building block in the creation of various organic compounds. In organic synthesis, 2-(4-Bromophenyl)-1H-indole is frequently employed as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and materials science applications. Due to its bromine substitution, this compound provides a convenient site for further derivatization, enabling the introduction of diverse functional groups to tailor the molecule's properties for specific applications. With its strategic placement of the bromine atom and indole core, 2-(4-Bromophenyl)-1H-indole offers chemists a powerful tool for designing and synthesizing complex molecules with enhanced biological or material properties.