N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

Base Information

Chemical Name:N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine
CAS No.:87948-01-4
Molecular Formula:C12H13 N3 O
Molecular Weight:215.25112
Hs Code.:2933990090
DSSTox Substance ID:DTXSID30522821
Wikidata:Q82388441
Mol file:87948-01-4.mol

Synonyms:87948-01-4;N-(2-ACETYLAMINOPHENYL)-1H-PYRROL-1-AMINE;N-[2-(PYRROL-1-YLAMINO)PHENYL]ACETAMIDE;N-(2-((1H-Pyrrol-1-yl)amino)phenyl)acetamide;N-{2-[(1H-Pyrrol-1-yl)amino]phenyl}acetamide;DTXSID30522821;AKOS015964980

Suppliers and Price of N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

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
Packaging
price

American Custom Chemicals Corporation
N-(2-ACETYLAMINOPHENYL)-1H-PYRROL-1-AMINE 95.00%
5MG
$ 504.72

Total 6 raw suppliers

Chemical Property of N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

Chemical Property:

Refractive Index:1.6
PSA：46.06000
Density:1.16g/cm³
LogP:2.46770
XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:215.105862047
Heavy Atom Count:16
Complexity:238

Purity/Quality:

98% ^*data from raw suppliers

N-(2-ACETYLAMINOPHENYL)-1H-PYRROL-1-AMINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=CC=C1NN2C=CC=C2

Technology Process of N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

There total 3 articles about N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine 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: 84.0%

: 87948-00-3
N-(2-Aminophenyl)-1H-pyrrol-1-amine

: 75-36-5
acetyl chloride

: 87948-01-4
N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

Guidance literature:: With triethylamine; In tetrahydrofuran; for 1h; Ambient temperature;
DOI:10.1055/s-1983-30503

Reference yield:

: 79700-48-4
N-(2-nitrophenyl)-1H-pyrrol-1-ylamine

: 87948-01-4
N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / H₂ / 10percent Pd/C / ethyl acetate / 4 h / 3040 Torr / Ambient temperature

2: 84 percent / triethylamine / tetrahydrofuran / 1 h / Ambient temperature

With hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;
DOI:10.1055/s-1983-30503

Reference yield:

: 3034-19-3
(2-nitrophenyl)hydrazine

: 87948-01-4
N-(2-Acetylaminophenyl)-1H-pyrrol-1-amine

Guidance literature:: Multi-step reaction with 3 steps

1: 79 percent / HCl(g) / ethanol / 0.5 h / Heating

2: 81 percent / H₂ / 10percent Pd/C / ethyl acetate / 4 h / 3040 Torr / Ambient temperature

3: 84 percent / triethylamine / tetrahydrofuran / 1 h / Ambient temperature

With hydrogenchloride; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; ethyl acetate;
DOI:10.1055/s-1983-30503