3-Methyl-2-(4-nitrophenyl)benzofuran

Base Information

Chemical Name:3-Methyl-2-(4-nitrophenyl)benzofuran
CAS No.:32437-49-3
Molecular Formula:C15H11NO3
Molecular Weight:253.257
Hs Code.:
DSSTox Substance ID:DTXSID801290858
Nikkaji Number:J678.856D
Mol file:32437-49-3.mol

Synonyms:3-Methyl-2-(4-nitrophenyl)benzofuran;DTXSID801290858;32437-49-3

Suppliers and Price of 3-Methyl-2-(4-nitrophenyl)benzofuran

Supply Marketing:

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

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Chemical Property of 3-Methyl-2-(4-nitrophenyl)benzofuran

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:253.07389321
Heavy Atom Count:19
Complexity:333

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(OC2=CC=CC=C12)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 3-Methyl-2-(4-nitrophenyl)benzofuran

There total 6 articles about 3-Methyl-2-(4-nitrophenyl)benzofuran 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: 58.0%

: 32437-48-2
o-(p-nitrobenzyloxy)acetophenone

: 32437-49-3
3-methyl-2-(4-nitrophenyl)benzofuran

Guidance literature:: With aluminum oxide; alkali metal fluoride; In N,N-dimethyl-formamide; at 110 ℃; for 4h;
DOI:10.1055/s-1995-4057

Reference yield: 35.0%

: C₉H₈N₂O₅

: 118-93-4,104809-67-8
o-hydroxyacetophenone

: 32437-49-3
3-methyl-2-(4-nitrophenyl)benzofuran

Guidance literature:: o-hydroxyacetophenone; With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 0.166667h;

C₉H₈N₂O₅; In N,N-dimethyl-formamide; at 110 ℃; for 12h;
DOI:10.1021/acs.joc.1c00143