4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde

Base Information

Chemical Name:4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde
CAS No.:128843-62-9
Molecular Formula:C₁₄H₁₃NO₃
Molecular Weight:243.262
Hs Code.:
DSSTox Substance ID:DTXSID401196743

Synonyms:DTXSID401196743;AKOS000345145;4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde;128843-62-9

Suppliers and Price of 4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde

Supply Marketing:

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

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Chemical Property of 4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:4
Exact Mass:243.08954328
Heavy Atom Count:18
Complexity:310

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CN1C=C(C=C1C=O)C(=O)C2=CC=C(C=C2)OC

Technology Process of 4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde

There total 3 articles about 4-(4-Methoxybenzoyl)-1-methyl-1H-pyrrole-2-carboxaldehyde 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:

: 96-54-8
N-Methylpyrrole

: 100-07-2
4-methoxy-benzoyl chloride

: 68-12-2,33513-42-7
N,N-dimethyl-formamide

: 128843-62-9
4-(4-Methoxy-benzoyl)-1-methyl-1H-pyrrole-2-carbaldehyde

Guidance literature:: Yield given. Multistep reaction;
DOI:10.1021/jm00172a026

Reference yield:

: 96-54-8
N-Methylpyrrole

: 128843-62-9
4-(4-Methoxy-benzoyl)-1-methyl-1H-pyrrole-2-carbaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl chloride / 1,2-dichloro-ethane / 0.25 h / 20 °C

2: AlCl₃ / 1,2-dichloro-ethane / 3 h

With aluminium trichloride; oxalyl dichloride; In 1,2-dichloro-ethane; 1: Vilsmeier-Haack reaction / 2: Friedel-Crafts reaction;
DOI:10.1021/jm021070e