1. Home
  2. 1H-Indole, 7-methoxy-2-phenyl-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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, 7-methoxy-2-phenyl-

COc1cccc2c1[nH]c(c2)c1ccccc1 Request for Quotation
Chemical Name: 1H-Indole, 7-methoxy-2-phenyl-
CAS Number: 66354-88-9
Product Number: AG00FXC4(AGN-PC-0NIWPK)
Synonyms:
MDL No:
Molecular Formula: C15H13NO
Molecular Weight: 223.26982

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


7-Methoxy-2-phenyl-1H-indole, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structure and reactivity. This compound is commonly used in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its presence allows for the introduction of the indole moiety in organic molecules, imparting desirable properties and functionalities.In chemical synthesis, 7-Methoxy-2-phenyl-1H-indole can be utilized for the preparation of heterocyclic compounds, such as indole derivatives, which are widely employed in medicinal chemistry and drug discovery. Its methoxy and phenyl groups provide strategic handles for further modification, enabling the creation of novel compounds with potentially enhanced biological activities.Furthermore, the indole scaffold of 7-Methoxy-2-phenyl-1H-indole lends itself well to diversification through various synthetic methodologies, including functional group transformations, cross-coupling reactions, and heterocycle formations. This versatility makes it a valuable building block for the synthesis of complex organic molecules with diverse structures and properties.Overall, 7-Methoxy-2-phenyl-1H-indole plays a crucial role in chemical synthesis by enabling the efficient construction of biologically relevant compounds and facilitating the development of new drug candidates and materials.