1H-Indole-3-ethanol,7-methoxy-

Base Information

• Chemical Name: 1H-Indole-3-ethanol,7-methoxy-
• CAS No.: 39232-86-5
• Molecular Formula: C11H13NO2
• Molecular Weight: 191.22600
• DSSTox Substance ID: DTXSID401308124
• Mol file: 39232-86-5.mol

Synonyms:39232-86-5;1H-INDOLE-3-ETHANOL,7-METHOXY-;2-(7-Methoxy-1H-indol-3-yl)ethan-1-ol;7-methoxytryptophol;2-(7-methoxy-1H-indol-3-yl)ethanol;7-Methoxy-1H-indole-3-ethanol;DTXSID401308124;PDSP1_001817;PDSP2_001800;AKOS006316096

Chemical Property of 1H-Indole-3-ethanol,7-methoxy-

Chemical Property:

• Boiling Point: 145 - 158 °C (0.1 mmHg)
• PSA: 45.25000
• LogP: 1.71130
• XLogP3: 1.6
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 191.094628657
• Heavy Atom Count: 14
• Complexity: 186

Purity/Quality:

99% ^*data from raw suppliers

1H-INDOLE-3-ETHANOL,7-METHOXY- 95 ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=CC2=C1NC=C2CCO

Technology Process of 1H-Indole-3-ethanol,7-methoxy-

There total 1 articles about 1H-Indole-3-ethanol,7-methoxy- 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:

→ 2-(7-methoxy-1H-indol-3-yl)ethanol (39232-86-5)

Guidance literature:

o-Methoxyphenylhydrazinhydrochlorid, 2,3-Dihydrofuran;

DOI:10.1007/BF00475537

Reference yield: 68.0%

α,α-diphenylindole-2-methanol (20538-21-0) + 2-(7-methoxy-1H-indol-3-yl)ethanol (39232-86-5) → 2-(2'-benzhydryl-7-methoxy-1H,1'H-[2,3'-biindol]-3-yl)ethanol

Guidance literature:

With toluene-4-sulfonic acid; In chloroform; at 50 ℃; for 12h; Green chemistry;

DOI:10.1039/c7ob03182c

Reference yield: 66.0%

(E)-diphenyl(3-styryl-1H-indol-2-yl)methanol + 2-(7-methoxy-1H-indol-3-yl)ethanol (39232-86-5) → 2-(7-methoxy-2-(2,3,3-triphenyl-1,2,3,4-tetrahydrocyclopenta[b]-indol-1-yl)-1H-indol-3-yl)ethanol

Guidance literature:

With toluene-4-sulfonic acid; In chloroform; at 40 ℃; for 8h; chemoselective reaction;

DOI:10.1021/acs.joc.8b00414

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