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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, 1-ethyl-2-phenyl-

CCn1c(cc2c1cccc2)c1ccccc1 Request for Quotation
Chemical Name: 1H-Indole, 1-ethyl-2-phenyl-
CAS Number: 13228-39-2
Product Number: AG0010HK(AGN-PC-0JLUEK)
Synonyms:
MDL No:
Molecular Formula: C16H15N
Molecular Weight: 221.2970

Identification/Properties

Properties
MP:
85-86 °C
BP:
390.6 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
221.303g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
0
Rotatable Bond Count:
2
Exact Mass:
221.12g/mol
Monoisotopic Mass:
221.12g/mol
Topological Polar Surface Area:
4.9A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
244
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Ethyl-2-phenyl-1H-indole, commonly known as $name$, is a versatile compound widely used in chemical synthesis. Due to its unique molecular structure, $name$ is a valuable building block in the creation of various organic compounds and pharmaceuticals. In chemical synthesis, $name$ serves as a key intermediate in the production of complex molecules. It can undergo various reactions such as Friedel-Crafts acylation, hydrogenation, and alkylation to generate compounds with diverse functionalities. Additionally, the presence of the indole moiety in the molecule imparts important biological properties to the final products, making it especially useful in the pharmaceutical industry.$name$ is often employed in the synthesis of heterocyclic compounds, natural products, and drug candidates. Its ability to introduce specific functional groups and stereochemistry enables chemists to tailor molecules for specific applications. Additionally, $name$ can be utilized in the development of new materials, agrochemicals, and advanced organic compounds.Overall, 1-Ethyl-2-phenyl-1H-indole plays a crucial role in modern chemical synthesis by providing a strategic starting point for the creation of complex and biologically active compounds. Its versatility and unique properties make it a valuable asset in the hands of chemists and researchers striving to develop innovative solutions in the field of organic chemistry.