(E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one

Base Information

Chemical Name:(E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one
CAS No.:15601-45-3
Molecular Formula:C₁₆H₁₀N₂O₄
Molecular Weight:294.266
Hs Code.:
European Community (EC) Number:652-065-5
Nikkaji Number:J402.042A,J543.917E

Synonyms:123990-32-9;(E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one;(4E)-4-[(3-nitrophenyl)methylidene]-2-phenyl-4,5-dihydro-1,3-oxazol-5-one;4-(3-Nitrobenzylidene)-2-phenyloxazol-5(4H)-one;15601-45-3;(4E)-4-[(3-nitrophenyl)methylidene]-2-phenyl-1,3-oxazol-5-one;AKOS000606284;2-Phenyl-4-[3-nitrobenzylidene]oxazol-5(4H)-one;F1425-0770;(4E)-4-(3-nitrobenzylidene)-2-phenyl-1,3-oxazol-5(4H)-one;2-Phenyl-4-[(E)-(3-nitrophenyl)methylene]-2-oxazolin-5-one

Suppliers and Price of (E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one

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 6 raw suppliers

Chemical Property of (E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one

Chemical Property:

Vapor Pressure:1.68E-08mmHg at 25°C
Boiling Point:456°C at 760 mmHg
Flash Point:229.6°C
Density:1.34g/cm³
XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:294.06405680
Heavy Atom Count:22
Complexity:515

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=NC(=CC3=CC(=CC=C3)[N+](=O)[O-])C(=O)O2
Isomeric SMILES:C1=CC=C(C=C1)C2=N/C(=C/C3=CC(=CC=C3)[N+](=O)[O-])/C(=O)O2

Technology Process of (E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one

There total 15 articles about (E)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one 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: 99.0%

: 495-69-2,140480-84-8,21251-67-2,91787-63-2,66407-11-2
Hippuric Acid

: 99-61-6
3-nitro-benzaldehyde

: 15601-45-3,66949-11-9,123990-32-9
(4Z)-4-(3-nitrobenzylidene)-2-phenyloxazol-5(4H)-one

Guidance literature:: With calcium acetate; acetic anhydride; at 45 - 47 ℃; for 0.0666667h; microwave irradiation;
DOI:10.1016/j.tetlet.2003.10.125

Reference yield: 98.0%

: 495-69-2,140480-84-8,21251-67-2,91787-63-2,66407-11-2
Hippuric Acid

: 99-61-6
3-nitro-benzaldehyde

: 15601-45-3,66949-11-9,123990-32-9
4-(3'-nitrobenzylidene)-2-phenyl-4-oxazolone

Guidance literature:: With acetic anhydride; 5-sulfosalicylic Acid; In water; at 20 ℃; for 0.533333h; Green chemistry;
DOI:10.3987/COM-17-13711

Reference yield: 96.0%

: 532-94-5
sodium hippurate

: 99-61-6
3-nitro-benzaldehyde

: 15601-45-3,66949-11-9,123990-32-9
4-(3'-nitrobenzylidene)-2-phenyl-4-oxazolone

Guidance literature:: With sodium acetate; acetic anhydride; triethylamine sulfate; In neat (no solvent); at 90 ℃; Green chemistry;
DOI:10.1080/00397911.2017.1340649