2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan

Base Information

Chemical Name:2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan
CAS No.:205113-79-7
Molecular Formula:C₁₈H₁₃ClO₂
Molecular Weight:296.753
Hs Code.:
DSSTox Substance ID:DTXSID901198087
Nikkaji Number:J938.815J

Synonyms:DTXSID901198087;205113-79-7;2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan;Methanone, (4-chlorophenyl)(2-methyl-5-phenyl-3-furanyl)-

Suppliers and Price of 2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan

Supply Marketing:

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

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Chemical Property of 2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan

Chemical Property:

XLogP3:5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:296.0604073
Heavy Atom Count:21
Complexity:356

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C=C(O1)C2=CC=CC=C2)C(=O)C3=CC=C(C=C3)Cl

Technology Process of 2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan

There total 1 articles about 2-Methyl-5-phenyl-3-(4-chlorobenzoyl)furan 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: 60.0%

: 108124-17-0
2-methyl-5-phenyl-furan-3-carboxylic acid

: 14774-78-8
4-chlorophenyl lithium

: 205113-79-7
p-chlorophenyl 2-methyl-5-phenyl-3-furyl ketone

Guidance literature:: In hexane; Ambient temperature;
DOI:10.1002/jhet.5570350114

Reference yield:

: 205113-79-7
p-chlorophenyl 2-methyl-5-phenyl-3-furyl ketone

: 4-(4-Chloro-phenyl)-2-phenyl-thieno[3,4-b]furan

Guidance literature:: Multi-step reaction with 2 steps

1: N-bromosuccinimide / CCl₄ / 4 h / Heating; Irradiation

2: 73 percent / thioacetamide / ethanol / 7 h / Heating

With N-Bromosuccinimide; thioacetamide; In tetrachloromethane; ethanol;
DOI:10.1002/jhet.5570350114