4,5-dimethoxy-1H-indole

Base Information

Chemical Name:4,5-dimethoxy-1H-indole
CAS No.:30933-67-6
Molecular Formula:C10H11 N O2
Molecular Weight:177.203
Hs Code.:2933990090
DSSTox Substance ID:DTXSID80365720
Wikidata:Q82150622
Mol file:30933-67-6.mol

Synonyms:4,5-dimethoxy-1H-indole;30933-67-6;4,5-dimethoxyindole;1H-Indole,4,5-dimethoxy-;SCHEMBL2085433;DTXSID80365720;XLORFNDUOILHCM-UHFFFAOYSA-N;MFCD03428582;AKOS006278634;AS-53714;P16936;A876064

Suppliers and Price of 4,5-dimethoxy-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

TRC
4,5-Dimethoxy-1H-indole
200mg
$ 175.00

Biosynth Carbosynth
4,5-Dimethoxyindole
1 g
$ 150.00

Biosynth Carbosynth
4,5-Dimethoxyindole
500 mg
$ 90.00

Biosynth Carbosynth
4,5-Dimethoxyindole
250 mg
$ 50.00

Biosynth Carbosynth
4,5-Dimethoxyindole
2 g
$ 250.00

AccelPharmtech
4,5-dimethoxy-1H-Indole 97.00%
25G
$ 5120.00

AccelPharmtech
4,5-dimethoxy-1H-Indole 97.00%
5G
$ 2750.00

AccelPharmtech
4,5-dimethoxy-1H-Indole 97.00%
1G
$ 2370.00

Total 10 raw suppliers

Chemical Property of 4,5-dimethoxy-1H-indole

Chemical Property:

Melting Point:160-161 °C
Boiling Point:320.3±22.0 °C(Predicted)
PKA:16.93±0.30(Predicted)
PSA：34.25000
Density:1.182±0.06 g/cm3(Predicted)
LogP:2.18510
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:177.078978594
Heavy Atom Count:13
Complexity:174

Purity/Quality:

97% ^*data from raw suppliers

4,5-Dimethoxy-1H-indole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C2=C(C=C1)NC=C2)OC

Technology Process of 4,5-dimethoxy-1H-indole

There total 9 articles about 4,5-dimethoxy-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: 90.0%

: 90916-24-8
2,3-dimethoxy-6,β-dinitrostyrene

: 30933-67-6
4,5-dimethoxy-1H-indole

Guidance literature:: With silica gel; iron; acetic acid; for 1h; Reflux;
DOI:10.1016/j.ejmech.2010.12.012

Reference yield: 83.0%

: 50536-49-7
4,5-dimethoxy-1H-indole-2-carboxylic acid

: 30933-67-6
4,5-dimethoxy-1H-indole

Guidance literature:: With quinoline; copper; Heating;
DOI:10.1021/jm0493616

Reference yield:

: 748717-43-3
1-Amino-o-homo-veratryl-alkohol

: 30933-67-6
4,5-dimethoxy-1H-indole

Guidance literature:: With potassium tert-butylate; calcium chloride; In o-xylene; at 140 ℃; for 12h; under 760.051 Torr; Inert atmosphere;
DOI:10.1039/c5ra16134g