(4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone

Base Information

Chemical Name:(4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone
CAS No.:92012-23-2
Molecular Formula:C19H17NO2
Molecular Weight:291.349
Hs Code.:
DSSTox Substance ID:DTXSID101188725

Synonyms:92012-23-2;(4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone;DTXSID101188725

Suppliers and Price of (4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone

Supply Marketing:

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

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Chemical Property of (4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:291.125928785
Heavy Atom Count:22
Complexity:356

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C(=O)C2=CC=C(N2)CC3=CC=CC=C3

Technology Process of (4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone

There total 2 articles about (4-Methoxyphenyl)[5-(phenylmethyl)-1H-pyrrol-2-yl]methanone 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:

: 7697-46-3
phenyl(1H-pyrrol-2-yl)methanone

: 92012-23-2
2-(4-Methoxybenzoyl)-5-benzylpyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / lithium aluminum hydride / tetrahydrofuran / 48 h / Heating

2: 1) phosphorus oxychloride / 1) 5h, room temperature 2) dry 1,2-dichloroethane, 15h

With lithium aluminium tetrahydride; trichlorophosphate; In tetrahydrofuran;
DOI:10.1021/jo00196a020

Reference yield:

: 7504-58-7
N-(4-methoxybenzoyl)morpholine

: 33234-48-9
2-benzyl-1H-pyrrole

: 92012-23-2
2-(4-Methoxybenzoyl)-5-benzylpyrrole

Guidance literature:: With trichlorophosphate; Yield given. Multistep reaction; 1) 5h, room temperature 2) dry 1,2-dichloroethane, 15h;
DOI:10.1021/jo00196a020