5-acetyl-1H-indole-3-carboxylic acid

Base Information

Chemical Name:5-acetyl-1H-indole-3-carboxylic acid
CAS No.:626234-82-0
Molecular Formula:C11H9NO3
Molecular Weight:203.197
Hs Code.:
DSSTox Substance ID:DTXSID00697378
Wikidata:Q82627263
Mol file:626234-82-0.mol

Synonyms:5-acetyl-1H-indole-3-carboxylic acid;626234-82-0;5-acetylindole-3-carboxylic acid;H-ORN-ORN-ORN-OHACOH;DTXSID00697378;FT-0704902

Suppliers and Price of 5-acetyl-1H-indole-3-carboxylic 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

AccelPharmtech
5-acetyl-1H-Indole-3-carboxylicacid 97.00%
5G
$ 2750.00

Total 7 raw suppliers

Chemical Property of 5-acetyl-1H-indole-3-carboxylic acid

Chemical Property:

PSA：70.16000
LogP:2.06870
XLogP3:1.7
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:203.058243149
Heavy Atom Count:15
Complexity:290

Purity/Quality:

98%min ^*data from raw suppliers

5-acetyl-1H-Indole-3-carboxylicacid 97.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CC2=C(C=C1)NC=C2C(=O)O

Technology Process of 5-acetyl-1H-indole-3-carboxylic acid

There total 3 articles about 5-acetyl-1H-indole-3-carboxylic 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: 98.0%

: 626234-71-7
5-acetyl-3-trifluoroacetylindole

: 626234-82-0
5-acetylindole-3-carboxylic acid

Guidance literature:: With potassium hydroxide; Heating;
DOI:10.1055/s-2003-40864

Reference yield:

: 14618-45-2
2,2,2-trifluoro-1-(1H-indol-3-yl)ethanone

: 626234-82-0
5-acetylindole-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / AlCl₃ / nitromethane / 4 h / 20 °C

2: 98 percent / aq. KOH / Heating

With potassium hydroxide; aluminium trichloride; In nitromethane; 1: Friedel-Crafts acylation;
DOI:10.1055/s-2003-40864