N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide

Base Information

Chemical Name:N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide
CAS No.:3388-98-5
Molecular Formula:C12H12N2O
Molecular Weight:200.24
Hs Code.:
DSSTox Substance ID:DTXSID40493932

Synonyms:3388-98-5;N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide;N-[2-(1H-Pyrrol-1-yl)phenyl]acetamide;SCHEMBL4789375;DTXSID40493932;HMS3446F09;AKOS025204409

Suppliers and Price of N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide

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

Total 1 raw suppliers

Chemical Property of N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:200.094963011
Heavy Atom Count:15
Complexity:224

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)NC1=CC=CC=C1N2C=CC=C2

Technology Process of N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide

There total 9 articles about N-(2-(1H-Pyrrol-1-yl)phenyl)acetamide 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: 93.0%

: 6025-60-1
2-(1H-pyrrol-1-yl)aniline

: 108-24-7
acetic anhydride

: 3388-98-5
2–(1H–pyrrol–1–yl)acetanilide

Guidance literature:: With acetic acid; at 120 ℃; for 0.333333h;
DOI:10.1002/cmdc.202000446

Reference yield: 67.0%

: 6025-60-1
2-(1H-pyrrol-1-yl)aniline

: 75-36-5
acetyl chloride

: 3388-98-5
2–(1H–pyrrol–1–yl)acetanilide

Guidance literature:: With pyridine; In 1,4-dioxane; for 4h; Heating;
DOI:10.1016/j.bmc.2006.09.068

Reference yield:

: 33265-60-0
1-(2-nitrophenyl)-1H-pyrrole

: 3388-98-5
2–(1H–pyrrol–1–yl)acetanilide

Guidance literature:: Multi-step reaction with 2 steps

1: BiCl₃; NaBH₄ / ethanol

2: 67 percent / pyridine / dioxane / 4 h / Heating

With pyridine; bismuth(III) chloride; sodium tetrahydroborate; In 1,4-dioxane; ethanol;
DOI:10.1016/j.bmc.2006.09.068