2-Benzoyl-5-methoxy-1H-indole-3-carboxylic acid

Base Information

Chemical Name:2-Benzoyl-5-methoxy-1H-indole-3-carboxylic acid
CAS No.:74588-83-3
Molecular Formula:C₁₇H₁₃NO₄
Molecular Weight:295.295
Hs Code.:
DSSTox Substance ID:DTXSID40503282
Wikidata:Q82356968

Synonyms:2-Benzoyl-5-methoxy-1H-indole-3-carboxylic acid;74588-83-3;DTXSID40503282

Suppliers and Price of 2-Benzoyl-5-methoxy-1H-indole-3-carboxylic acid

Supply Marketing:

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

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Chemical Property of 2-Benzoyl-5-methoxy-1H-indole-3-carboxylic acid

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:295.08445790
Heavy Atom Count:22
Complexity:432

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)NC(=C2C(=O)O)C(=O)C3=CC=CC=C3

Technology Process of 2-Benzoyl-5-methoxy-1H-indole-3-carboxylic acid

There total 3 articles about 2-Benzoyl-5-methoxy-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:

: 39755-95-8
5-methoxyisatine

: 74588-83-3
5-methoxy-2-benzoylindolyl-3-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: NaOH / methanol

2: dimethylformamide

3: 20percent aq. NaOH / 12 h / Heating

With sodium hydroxide; In methanol; N,N-dimethyl-formamide;
DOI:10.1039/c39800000200

Reference yield:

: Sodium; (2-amino-5-methoxy-phenyl)-oxo-acetate

: 74588-83-3
5-methoxy-2-benzoylindolyl-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: dimethylformamide

2: 20percent aq. NaOH / 12 h / Heating

With sodium hydroxide; In N,N-dimethyl-formamide;
DOI:10.1039/c39800000200