4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide

Base Information

Chemical Name:4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide
CAS No.:50371-36-3
Molecular Formula:C11H7Br3N2O
Molecular Weight:422.901
Hs Code.:
DSSTox Substance ID:DTXSID60606007
Wikidata:Q82504521

Synonyms:50371-36-3;4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide;SCHEMBL11607016;DTXSID60606007

Suppliers and Price of 4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of 4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide

Chemical Property:

XLogP3:4.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:421.80880
Heavy Atom Count:17
Complexity:290

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Br)NC(=O)C2=CC(=C(N2)Br)Br

Technology Process of 4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide

There total 3 articles about 4,5-Dibromo-N-(3-bromophenyl)-1H-pyrrole-2-carboxamide 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:

: 34649-21-3
4,5-dibromo-1H-pyrrole-2-carboxylic acid

: 591-19-5
m-Bromoaniline

: 50371-36-3
3',4,5-tribromopyrrole-2-carboxanilide

Guidance literature:: With thionyl chloride; In pyridine; benzene;

Reference yield:

: 35302-72-8
pyrrol-2-yl trichloromethyl ketone

: 50371-36-3
3',4,5-tribromopyrrole-2-carboxanilide

Guidance literature:: Multi-step reaction with 3 steps

1: bromine / acetic acid

2: sodium hydroxide; water

3: thionyl chloride / pyridine; benzene

With thionyl chloride; bromine; In pyridine; sodium hydroxide; water; acetic acid; benzene;