2-(7-methoxy-1H-indol-3-yl)acetic Acid

Base Information

Chemical Name:2-(7-methoxy-1H-indol-3-yl)acetic Acid
CAS No.:850008-37-6
Molecular Formula:C11H11 N O3
Molecular Weight:205.21
Hs Code.:2933990090
DSSTox Substance ID:DTXSID00471332
Wikidata:Q82299823
Mol file:850008-37-6.mol

Synonyms:2-(7-methoxy-1H-indol-3-yl)acetic Acid;850008-37-6;(7-Methoxy-1H-indol-3-yl)acetic acid;2-(7-METHOXYINDOL-1H-3-YL)ACETIC ACID;SCHEMBL21808835;DTXSID00471332;AKOS022211950;KS-9245;CS-0235869;2-(7-METHOXYINDOL-1H-3-YL)ACETICACID;EN300-1635712

Suppliers and Price of 2-(7-methoxy-1H-indol-3-yl)acetic Acid

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

AK Scientific
2-(7-Methoxy-1H-indol-3-yl)aceticAcid
5g
$ 6531.00

AK Scientific
2-(7-Methoxy-1H-indol-3-yl)aceticAcid
1g
$ 2319.00

AK Scientific
2-(7-Methoxy-1H-indol-3-yl)aceticAcid
5mg
$ 303.00

Total 5 raw suppliers

Chemical Property of 2-(7-methoxy-1H-indol-3-yl)acetic Acid

Chemical Property:

PSA：62.32000
LogP:1.80360
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:205.07389321
Heavy Atom Count:15
Complexity:244

Purity/Quality:

99% ^*data from raw suppliers

2-(7-Methoxy-1H-indol-3-yl)aceticAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC2=C1NC=C2CC(=O)O

Technology Process of 2-(7-methoxy-1H-indol-3-yl)acetic Acid

There total 6 articles about 2-(7-methoxy-1H-indol-3-yl)acetic Acid 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: 100.0%

: 1067080-51-6
C₁₂H₁₃NO₃

: 850008-37-6
7-methoxyindoleacetic acid

Guidance literature:: With potassium hydroxide; In tetrahydrofuran; water; at 20 ℃;
DOI:10.1016/j.phytochem.2007.04.030

Reference yield:

: 3189-22-8
7-methoxy-1H-indole

: 850008-37-6
7-methoxyindoleacetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 2 h / 0 °C

2: triethylamine / tetrahydrofuran / 4 h / 20 °C

3: 96 percent / NaH₂PO₂*H₂O / palladium on activated charcoal / dioxane; H₂O / 48 h / 20 °C

4: 100 percent / KOH / tetrahydrofuran; H₂O / 20 °C

With potassium hydroxide; sodium hypophosphite; triethylamine; isobutyric Acid; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; water;
DOI:10.1016/j.phytochem.2007.04.030

Reference yield:

: 50656-47-8
7-methoxyindole-3-glyoxyl chloride

: 850008-37-6
7-methoxyindoleacetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / tetrahydrofuran / 4 h / 20 °C

2: 96 percent / NaH₂PO₂*H₂O / palladium on activated charcoal / dioxane; H₂O / 48 h / 20 °C

3: 100 percent / KOH / tetrahydrofuran; H₂O / 20 °C

With potassium hydroxide; sodium hypophosphite; triethylamine; isobutyric Acid; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; water;
DOI:10.1016/j.phytochem.2007.04.030