Phenyl(2-phenyl-1H-indol-1-yl)methanone

Base Information

• Chemical Name: Phenyl(2-phenyl-1H-indol-1-yl)methanone
• CAS No.: 53330-45-3
• Molecular Formula: C21H15NO
• Molecular Weight: 297.356
• ChEMBL ID: CHEMBL2271981
• DSSTox Substance ID: DTXSID10527859
• Nikkaji Number: J2.857.692G
• Wikidata: Q82397079
• Mol file: 53330-45-3.mol

Synonyms:Phenyl(2-phenyl-1H-indol-1-yl)methanone;1-benzoyl-2-phenyl-1H-indole;53330-45-3;CHEMBL2271981;SCHEMBL14525877;DTXSID10527859;phenyl-(2-phenyl-1H-indol-1-yl)-methanone

Chemical Property of Phenyl(2-phenyl-1H-indol-1-yl)methanone

Chemical Property:

• XLogP3: 5.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 297.115364102
• Heavy Atom Count: 23
• Complexity: 408

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=CC3=CC=CC=C3N2C(=O)C4=CC=CC=C4

Technology Process of Phenyl(2-phenyl-1H-indol-1-yl)methanone

There total 16 articles about Phenyl(2-phenyl-1H-indol-1-yl)methanone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 94.0%

N-(2-(2-phenylethynyl)phenyl)benzamide (104682-98-6) → phenyl(2-phenyl-1H-indol-1-yl)methanone (53330-45-3)

Guidance literature:

With methyl vinyl ketone; palladium dichloride; In acetonitrile; at 60 ℃; for 24h; Inert atmosphere;

DOI:10.1016/j.tet.2013.01.081

Reference yield: 84.0%

N-(2-(1-phenylvinyl)phenyl)benzamide (1392323-07-7) → phenyl(2-phenyl-1H-indol-1-yl)methanone (53330-45-3)

Guidance literature:

With camphor-10-sulfonic acid; In acetonitrile; at 60 ℃; for 18h;

DOI:10.1021/jacs.8b08350

Reference yield: 71.0%

N-(4-cyano-2-(2-oxopropyl)phenyl)acetamide → phenyl(2-phenyl-1H-indol-1-yl)methanone (53330-45-3)

Guidance literature:

With iron(III) chloride; In acetonitrile; at 90 ℃; for 12h; Schlenk technique;

DOI:10.1002/chem.201500272

upstream raw materials:

N-(2-(2-phenylethynyl)phenyl)benzamide

1-bromo-2-(phenylethenyl)benzene

benzamide

phenylacetylene

Downstream raw materials:

2-phenyl-indole

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