7-ethoxy-1H-indole

Base Information

Chemical Name:7-ethoxy-1H-indole
CAS No.:927181-96-2
Molecular Formula:C10H11NO
Molecular Weight:161.203
Hs Code.:2933990090
DSSTox Substance ID:DTXSID40600583
Wikidata:Q72471681
Mol file:927181-96-2.mol

Synonyms:7-Ethoxyindole;7-ethoxy-1H-indole;927181-96-2;SCHEMBL593890;DTXSID40600583;UOFKEBQFRTULGS-UHFFFAOYSA-N;AKOS006306412;AC-27783;DB-079389;CS-0086866;A816391;A1-03122

Suppliers and Price of 7-ethoxy-1H-indole

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

Crysdot
7-Ethoxy-1H-indole 97%
5g
$ 652.00

ChemScene
7-Ethoxy-1H-indole
100mg
$ 138.00

ChemScene
7-Ethoxy-1H-indole
5g
$ 1390.00

ChemScene
7-Ethoxy-1H-indole
1g
$ 462.00

ChemScene
7-Ethoxy-1H-indole
250mg
$ 230.00

Chemenu
7-Ethoxyindole 95%+
5g
$ 615.00

American Custom Chemicals Corporation
7-ETHOXYINDOLE 95.00%
10G
$ 1334.03

American Custom Chemicals Corporation
7-ETHOXYINDOLE 95.00%
5G
$ 909.56

Alichem
7-Ethoxyindole
1g
$ 213.07

Alichem
7-Ethoxyindole
5g
$ 745.73

Total 17 raw suppliers

Chemical Property of 7-ethoxy-1H-indole

Chemical Property:

Vapor Pressure:0.001mmHg at 25°C
Boiling Point:309.008oC at 760 mmHg
Flash Point:113.308oC
PSA：25.02000
Density:1.132g/cm3
LogP:2.56660
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:161.084063974
Heavy Atom Count:12
Complexity:149

Purity/Quality:

NLT 98% ^*data from raw suppliers

7-Ethoxy-1H-indole 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=CC=CC2=C1NC=C2

Technology Process of 7-ethoxy-1H-indole

There total 1 articles about 7-ethoxy-1H-indole 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:

: 2380-84-9
7-Indolol

: 75-03-6
ethyl iodide

: 927181-96-2
7-ethoxy-1H-indole

Guidance literature:: With potassium carbonate; potassium iodide; In N,N-dimethyl-formamide; at 90 ℃;
DOI:10.1248/cpb.53.184

Reference yield:

: 927181-96-2
7-ethoxy-1H-indole

: (1R)-(3-chlorophenyl)-2-[(7-ethoxy-1H-indol-3-yl)prop-2-ylamino]ethanol

Guidance literature:: Multi-step reaction with 4 steps

1: phosphorus oxychloride / 2 h / 20 °C

2: ammonium acetate; Ac₂O; AcOH / AcONa / 2 h / Heating

3: LiAlH₄ / tetrahydrofuran; diethyl ether / 5.5 h / Heating

4: methanol / 20 °C

With ammonium acetate; lithium aluminium tetrahydride; acetic anhydride; acetic acid; trichlorophosphate; sodium acetate; In tetrahydrofuran; methanol; diethyl ether; 1: Vilsmeier reaction;
DOI:10.1248/cpb.53.184

Reference yield:

: 927181-96-2
7-ethoxy-1H-indole

: 179819-92-2
3-(2-aminopropyl)-7-ethoxyindole

Guidance literature:: Multi-step reaction with 3 steps

1: phosphorus oxychloride / 2 h / 20 °C

2: ammonium acetate; Ac₂O; AcOH / AcONa / 2 h / Heating

3: LiAlH₄ / tetrahydrofuran; diethyl ether / 5.5 h / Heating

With ammonium acetate; lithium aluminium tetrahydride; acetic anhydride; acetic acid; trichlorophosphate; sodium acetate; In tetrahydrofuran; diethyl ether; 1: Vilsmeier reaction;
DOI:10.1248/cpb.53.184