2-Furyl(4-methylphenyl)methanone

Base Information

Chemical Name:2-Furyl(4-methylphenyl)methanone
CAS No.:13365-62-3
Molecular Formula:C12H10O2
Molecular Weight:186.21
Hs Code.:2932190090
DSSTox Substance ID:DTXSID50546943
Nikkaji Number:J1.399.049B
Wikidata:Q82424911
Mol file:13365-62-3.mol

Synonyms:13365-62-3;2-FURYL(4-METHYLPHENYL)METHANONE;Furan-2-yl(p-tolyl)methanone;furan-2-yl-(4-methylphenyl)methanone;CHEMBRDG-BB 6609577;SCHEMBL10682751;DTXSID50546943;(2-furanyl)-4-methylphenylmethanone;MFCD08691769;AKOS009500974;(Furan-2-yl)(4-methylphenyl)methanone;BS-37227;2-Furyl(4-methylphenyl)methanone, AldrichCPR

Suppliers and Price of 2-Furyl(4-methylphenyl)methanone

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

TRC
2-Furyl(4-methylphenyl)methanone
500mg
$ 110.00

TRC
2-Furyl(4-methylphenyl)methanone
100mg
$ 60.00

TRC
2-Furyl(4-methylphenyl)methanone
50mg
$ 45.00

ChemBridge Corporation
2-furyl(4-methylphenyl)methanone 95%
5 g
$ 133.00

Total 4 raw suppliers

Chemical Property of 2-Furyl(4-methylphenyl)methanone

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:313.727oC at 760 mmHg
Flash Point:144.425oC
PSA：30.21000
Density:1.118g/cm3
LogP:2.81900
XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:186.068079557
Heavy Atom Count:14
Complexity:204

Purity/Quality:

99% ^*data from raw suppliers

2-Furyl(4-methylphenyl)methanone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xn
Statements: 22

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=O)C2=CC=CO2

Technology Process of 2-Furyl(4-methylphenyl)methanone

There total 20 articles about 2-Furyl(4-methylphenyl)methanone 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: 95.0%

: 66117-64-4
di(p-tolyl)borinic acid

: N-methyl-N-tosylfuran-2-carboxamide

: 13365-62-3
furan-2-yl-p-tolyl-methanone

Guidance literature:: With [1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(ll) dichloride; potassium carbonate; In tetrahydrofuran; at 65 ℃; for 12h; Inert atmosphere; Schlenk technique;
DOI:10.1016/j.tetlet.2018.05.003

Reference yield: 92.0%

: 527-69-5
2-furancarbonyl chloride

: 5142-75-6
tri(p-tolyl)bismuth

: 13365-62-3
furan-2-yl-p-tolyl-methanone

Guidance literature:: With triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; at 80 ℃; for 3h;
DOI:10.1016/j.tet.2007.10.047

Reference yield: 89.0%

: 1467-70-5
furan-2-yl-oxo-acetic acid

: 624-31-7
4-tolyl iodide

: 13365-62-3
furan-2-yl-p-tolyl-methanone

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; potassium dihydrogenphosphate; [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; In N,N-dimethyl acetamide; at 25 ℃; for 20h; chemoselective reaction; Schlenk technique; Inert atmosphere; Irradiation;
DOI:10.1002/chem.201502286