1H-Indole, 2-(4-chlorophenyl)-3-phenyl-

Base Information

• Chemical Name: 1H-Indole, 2-(4-chlorophenyl)-3-phenyl-
• CAS No.: 144054-14-8
• Molecular Formula: C20H14ClN
• Molecular Weight: 303.791
• DSSTox Substance ID: DTXSID10459949
• Nikkaji Number: J2.032.469D
• Wikidata: Q82283842
• Mol file: 144054-14-8.mol

Synonyms:1H-Indole, 2-(4-chlorophenyl)-3-phenyl-;144054-14-8;1h-indole,2-(4-chlorophenyl)-3-phenyl-;2-(4-chlorophenyl)-3-phenyl-1H-indole;DTXSID10459949

Chemical Property of 1H-Indole, 2-(4-chlorophenyl)-3-phenyl-

Chemical Property:

• XLogP3: 6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 0
• Rotatable Bond Count: 2
• Exact Mass: 303.0814771
• Heavy Atom Count: 22
• Complexity: 357

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)C2=C(NC3=CC=CC=C32)C4=CC=C(C=C4)Cl

Technology Process of 1H-Indole, 2-(4-chlorophenyl)-3-phenyl-

There total 17 articles about 1H-Indole, 2-(4-chlorophenyl)-3-phenyl- 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: 88.0%

N-(2-Benzoyl-phenyl)-4-chloro-benzamide (144054-08-0) → 2-(4-chlorophenyl)-3-phenyl-1H-indole (144054-14-8)

Guidance literature:

With samarium diiodide; In tetrahydrofuran; at 65 ℃; for 0.833333h;

DOI:10.1016/S0040-4020(03)00143-1

Reference yield: 75.0%

N-(2-Benzoyl-phenyl)-4-chloro-benzamide (144054-08-0) → 2-(4-chlorophenyl)-3-phenyl-1H-indole (144054-14-8) + 2-(4-chlorophenyl)-3-phenyl-2,3-dihydro-1H-indole-2,3-diol

Guidance literature:

With samarium diiodide; In tetrahydrofuran; at -20 ℃; for 0.0833333h;

DOI:10.1016/S0040-4020(03)00143-1

Reference yield:

1-chloro-4-(2-phenylethynyl)benzene (5172-02-1) + 2-bromoaniline (615-36-1) → 2-(4-chlorophenyl)-3-phenyl-1H-indole (144054-14-8) + 3-(4-chlorophenyl)-2-phenyl-1H-indole (143360-82-1)

Guidance literature:

With lithium hydroxide monohydrate; C₂₄H₂₃N₃O₃PdS; In N,N-dimethyl-formamide; at 130 ℃; for 24h; Overall yield = 82 %; regioselective reaction;

DOI:10.1016/j.jorganchem.2013.05.049

upstream raw materials:

phenylhydrazine

4'-chloro-2-phenylacetophenone

N-(2-Benzoyl-phenyl)-4-chloro-benzamide

4-chloro-benzoyl chloride