1h-Indole,7-(triphenylmethoxy)-

Base Information

Chemical Name:1h-Indole,7-(triphenylmethoxy)-
CAS No.:135328-53-9
Molecular Formula:C₂₇H₂₁NO
Molecular Weight:375.47
Hs Code.:
DSSTox Substance ID:DTXSID801306906

Synonyms:135328-53-9;1h-indole,7-(triphenylmethoxy)-;7-trityloxyindole;SCHEMBL8303069;DWKRGTITPDSTEY-UHFFFAOYSA-N;DTXSID801306906;7-(TRIPHENYLMETHOXY)-1H-INDOLE

Suppliers and Price of 1h-Indole,7-(triphenylmethoxy)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 1 raw suppliers

Chemical Property of 1h-Indole,7-(triphenylmethoxy)-

Chemical Property:

XLogP3:6.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:375.162314293
Heavy Atom Count:29
Complexity:455

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)OC4=CC=CC5=C4NC=C5

Technology Process of 1h-Indole,7-(triphenylmethoxy)-

There total 4 articles about 1h-Indole,7-(triphenylmethoxy)- 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: 40.0%

: 1826-67-1
vinyl magnesium bromide

: 20499-26-7
1-Nitro-2-trityloxy-benzene

: 135328-53-9
7-trityloxyindole

Guidance literature:: In tetrahydrofuran; at -40 ℃; for 0.666667h;
DOI:10.1080/00397919108020827

Reference yield:

: 596-43-0
bromo-triphenyl-methane

: 135328-53-9
7-trityloxyindole

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 5 h / Heating

2: 40 percent / tetrahydrofuran / 0.67 h / -40 °C

With potassium carbonate; In tetrahydrofuran; acetone;
DOI:10.1080/00397919108020827

Reference yield:

: 88-75-5,78813-12-4
2-hydroxynitrobenzene

: 135328-53-9
7-trityloxyindole

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone / 5 h / Heating

2: 40 percent / tetrahydrofuran / 0.67 h / -40 °C

With potassium carbonate; In tetrahydrofuran; acetone;
DOI:10.1080/00397919108020827