1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde

Base Information

Chemical Name:1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde
CAS No.:477850-19-4
Molecular Formula:C11H8BrNO
Molecular Weight:250.095
Hs Code.:
DSSTox Substance ID:DTXSID00363268
Nikkaji Number:J2.438.907C
Wikidata:Q82146876

Synonyms:1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde;477850-19-4;1-(4-bromophenyl)pyrrole-3-carbaldehyde;10R-0654;SCHEMBL5126021;DTXSID00363268;CUA85019;MFCD02571988;AKOS005076175;SB63707

Suppliers and Price of 1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 1 raw suppliers

Chemical Property of 1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:248.97893
Heavy Atom Count:14
Complexity:202

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=CC=C1N2C=CC(=C2)C=O)Br

Technology Process of 1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde

There total 5 articles about 1-(4-bromophenyl)-1H-pyrrole-3-carbaldehyde 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: 64.0%

: 848317-67-9
[N-(4-bromophenyl)pyrrolidin-3-yl]methanol

: 477850-19-4
N-(4-bromophenyl)-3-formylpyrrole

Guidance literature:: With 2,3-dicyano-5,6-dichloro-p-benzoquinone; In benzene; for 8h; Heating;
DOI:10.1016/j.tetlet.2004.12.107

Reference yield:

: 226881-07-8
N-(4-bromophenyl)-2-oxo-pyrrolidine-3-carboxylic acid

: 477850-19-4
N-(4-bromophenyl)-3-formylpyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / NaBH₄; iodine / tetrahydrofuran / 2 h / 25 °C

2: 64 percent / DDQ / benzene / 8 h / 80 °C

With sodium tetrahydroborate; iodine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; benzene;
DOI:10.1016/j.tet.2007.01.058

Reference yield:

: 106-40-1
4-bromo-aniline

: 477850-19-4
N-(4-bromophenyl)-3-formylpyrrole

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / 25 °C

2: 81 percent / NaBH₄; iodine / tetrahydrofuran / 2 h / 25 °C

3: 64 percent / DDQ / benzene / 8 h / 80 °C

With sodium tetrahydroborate; iodine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; benzene;
DOI:10.1016/j.tet.2007.01.058