(4-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-yl)methanone

Base Information

Chemical Name:(4-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-yl)methanone
CAS No.:62128-48-7
Molecular Formula:C₁₄H₁₄ClNO
Molecular Weight:247.724
Hs Code.:
DSSTox Substance ID:DTXSID70505653
Wikidata:Q82360911

Synonyms:(4-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-yl)methanone;62128-48-7;DTXSID70505653;(4-chlorophenyl)-(1,2,4-trimethyl-1H-pyrrol-3-yl)-methanone

Suppliers and Price of (4-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-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-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-yl)methanone

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:247.0763918
Heavy Atom Count:17
Complexity:286

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CN(C(=C1C(=O)C2=CC=C(C=C2)Cl)C)C

Technology Process of (4-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-yl)methanone

There total 2 articles about (4-chlorophenyl)(1,2,4-trimethyl-1H-pyrrol-3-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: 44.0%

: 62128-28-3
2-(4-chlorobenzoyl)-1,3,5-trimethyl-1H-pyrrole

: 62128-48-7
3-(4-chlorobenzoyl)-1,2,4-trimethylpyrrole

Guidance literature:: With trifluorormethanesulfonic acid; trifluoroacetic acid; for 144h; Heating;
DOI:10.1021/jo00318a002

Reference yield:

: 33369-31-2
zomepirac

: 62128-48-7
3-(4-chlorobenzoyl)-1,2,4-trimethylpyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 19.2 g / propionic acid / 18 h / Heating

2: 44 percent / trifluoromethanesulfonic acid, trifluoroacetic acid / 144 h / Heating

With trifluorormethanesulfonic acid; propionic acid; trifluoroacetic acid;
DOI:10.1021/jo00318a002