5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)-

Base Information

Chemical Name:5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)-
CAS No.:111865-34-0
Molecular Formula:C14H8ClNO3
Molecular Weight:273.675
Hs Code.:
DSSTox Substance ID:DTXSID70385432
Mol file:111865-34-0.mol

Synonyms:WAY-312782;5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)-;DTXSID70385432

Suppliers and Price of 5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)-

Supply Marketing:

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

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Chemical Property of 5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)-

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:273.0192708
Heavy Atom Count:19
Complexity:424

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=COC(=C1)C=C2C(=O)OC(=N2)C3=CC=C(C=C3)Cl

Technology Process of 5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)-

There total 3 articles about 5(4H)-Oxazolone, 2-(4-chlorophenyl)-4-(2-furanylmethylene)- 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: 73.0%

: 122-01-0
4-chloro-benzoyl chloride

: 109547-79-7
C₂₇H₂₄NO₃P

: 111865-34-0
2-(4-chloro-phenyl)-4-furfuryliden-4H-oxazol-5-one

: 791-28-6
Triphenylphosphine oxide

Guidance literature:: In toluene; for 48h; Heating;

Reference yield:

: 35355-49-8
ethyl 2-azido-3-(furan-2-yl)acrylate

: 111865-34-0
2-(4-chloro-phenyl)-4-furfuryliden-4H-oxazol-5-one

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 0 °C

2: 73 percent / toluene / 48 h / Heating

In dichloromethane; toluene;