2-(di(1H-Indol-3-yl)methyl)phenol

Base Information

• Chemical Name: 2-(di(1H-Indol-3-yl)methyl)phenol
• CAS No.: 33948-97-9
• Molecular Formula: C23H18N2O
• Molecular Weight: 338.409
• ChEMBL ID: CHEMBL2376690
• DSSTox Substance ID: DTXSID60551442
• Nikkaji Number: J1.732.816F
• Wikidata: Q82431107

Synonyms:2-(di(1H-Indol-3-yl)methyl)phenol;33948-97-9;Phenol, 2-(di-1H-indol-3-ylmethyl)-;2-[BIS(1H-INDOL-3-YL)METHYL]PHENOL;2-[Di(1H-indol-3-yl)methyl]phenol;CHEMBL2376690;SCHEMBL20738931;DTXSID60551442

Chemical Property of 2-(di(1H-Indol-3-yl)methyl)phenol

Chemical Property:

• XLogP3: 5.2
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 338.141913202
• Heavy Atom Count: 26
• Complexity: 451

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C2C(=C1)C(=CN2)C(C3=CC=CC=C3O)C4=CNC5=CC=CC=C54

Technology Process of 2-(di(1H-Indol-3-yl)methyl)phenol

There total 8 articles about 2-(di(1H-Indol-3-yl)methyl)phenol 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: 97.0%

indole (120-72-9) + salicylaldehyde (90-02-8) → 3-[(1H-indol-3-yl)(2-hydroxyphenyl)methyl]-1H-indole (33948-97-9)

Guidance literature:

With [N,N′-bis(salicylidene)-1,2-phenylenediamine]chloridoiron(III); tetrabutylammomium bromide; at 110 ℃; for 0.5h;

DOI:10.1002/cjoc.201090119

Reference yield: 95.0%

indole (120-72-9) + 2-methyl-benzyl alcohol (89-95-2) → 3-[(1H-indol-3-yl)(2-hydroxyphenyl)methyl]-1H-indole (33948-97-9)

Guidance literature:

With Montmorillonite K₁₀ clay; at 20 ℃; for 2h;

DOI:10.1016/S0040-4039(02)00682-2

Reference yield: 93.0%

indole (120-72-9) + 2-hydroxybenzaldehyde phenylhydrazone (614-65-3) → 3-[(1H-indol-3-yl)(2-hydroxyphenyl)methyl]-1H-indole (33948-97-9)

Guidance literature:

With Fe⁺³-montmorillonite K₁₀; for 0.025h;

DOI:10.1134/S1070363215120361

upstream raw materials:

indole

N-phenylsalicylaldimine

2-methyl-benzyl alcohol

salicylaldehyde

Downstream raw materials:

indole

C₄₈H₈₀O₄₀*C₂₃H₁₈N₂O

C₃₆H₆₀O₃₀*C₂₃H₁₈N₂O

C₄₂H₇₀O₃₅*C₂₃H₁₈N₂O

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