N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide

Base Information

Chemical Name:N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide
CAS No.:37056-75-0
Molecular Formula:C₁₅H₁₃NO
Molecular Weight:223.274
Hs Code.:
NSC Number:152376
ChEMBL ID:CHEMBL3192129
Mol file:37056-75-0.mol

Synonyms:MLS000766168;NSC152376;CHEMBL3192129;SCHEMBL13164321;HMS2884B16;N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide;STL020676;AKOS002316182;NSC-152376;37056-75-0;SMR000528643

Suppliers and Price of N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide

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 5 raw suppliers

Chemical Property of N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide

Chemical Property:

Vapor Pressure:3.84E-06mmHg at 25°C
Boiling Point:396.7°C at 760 mmHg
Flash Point:187.9°C
Density:1.119g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:223.099714038
Heavy Atom Count:17
Complexity:271

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)C=CC=[N+](C2=CC=CC=C2)[O-]
Isomeric SMILES:C1=CC=C(C=C1)/C=C/C=[N+](/C2=CC=CC=C2)\[O-]

Technology Process of N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide

There total 11 articles about N-phenyl-N-[(1Z,2E)-3-phenylprop-2-en-1-ylidene]amine oxide 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: 100.0%

: 100-65-2
N-Phenylhydroxylamine

: 104-55-2
3-phenyl-propenal

: 37056-75-0,1070670-27-7
cinnamaldehyde-(N-phenyl oxime )

Guidance literature:: In chloroform; at 0 ℃;
DOI:10.1007/BF00475373

Reference yield: 83.0%

: 495-48-7,55599-32-1
azoxybenzene

: 14371-10-9
(E)-3-phenylpropenal

: 37056-75-0,1070670-27-7
cinnamaldehyde-(N-phenyl oxime )

Guidance literature:: With acetaldehyde enolate; ammonium chloride; In tetrahydrofuran; 1) reflux, 1 h, 2) r.t., 10 min.; also with K₂CO₃ or MeO^- as base;
DOI:10.1016/S0040-4020(01)86449-8