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(NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine

Base Information Edit
  • Chemical Name:(NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine
  • CAS No.:40143-27-9
  • Molecular Formula:C13H11 N O
  • Molecular Weight:197.236
  • Hs Code.:2928000090
  • NSC Number:93959
  • Nikkaji Number:J1.113.931K
  • Mol file:40143-27-9.mol
(NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine

Synonyms:(NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine;40143-27-9;NSC93959;4-Biphenylaldehydeoxime;Biphenyl-4-carbaldehydeoxime;SCHEMBL4686720;(E)-biphenyl-4-carbaldehyde oxime;NSC-93959;1089301-82-5

Suppliers and Price of (NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine
Supply Marketing:Edit
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
  • 4-Phenylbenzaldoxime
  • 2.5g
  • $ 85.00
  • Sigma-Aldrich
  • 4-Phenylbenzaldoxime analytical standard
  • 1g
  • $ 45.50
  • Crysdot
  • [1,1'-Biphenyl]-4-carbaldehydeoxime 97%
  • 5g
  • $ 805.00
  • AHH
  • 4-Biphenylaldehydeoxime 96%
  • 50g
  • $ 310.00
Total 11 raw suppliers
Chemical Property of (NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine Edit
Chemical Property:
  • Vapor Pressure:4.92E-05mmHg at 25°C 
  • Boiling Point:334.8°Cat760mmHg 
  • Flash Point:206.9°C 
  • PSA:32.59000 
  • Density:1.05g/cm3 
  • LogP:3.16170 
  • XLogP3:3.7
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:197.084063974
  • Heavy Atom Count:15
  • Complexity:201
Purity/Quality:

98%,99%, *data from raw suppliers

4-Phenylbenzaldoxime *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C2=CC=C(C=C2)C=NO
  • Isomeric SMILES:C1=CC=C(C=C1)C2=CC=C(C=C2)/C=N\O
  • Uses 4-Phenylbenzaldoxime is a reactant in the design and synthesis of substituted-isoxazole derivatives as farnesoid X receptor (FXR) antagonists.
Technology Process of (NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine

There total 4 articles about (NZ)-N-[(4-phenylphenyl)methylidene]hydroxylamine 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:
Guidance literature:
With hydroxylamine hydrochloride; sodium carbonate; In methanol; water; at 20 ℃; for 3h;
DOI:10.1039/c6ra02222g
Guidance literature:
4-bromo-1,1'-biphenyl; With n-butyllithium; In tetrahydrofuran; hexane; at -50 ℃; for 0.5h; Inert atmosphere;
N,N-dimethyl-formamide; In tetrahydrofuran; hexane; at -50 - 20 ℃; for 1h; Inert atmosphere;
With hydroxylamine hydrochloride; potassium carbonate; In tetrahydrofuran; hexane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tet.2018.06.044
Guidance literature:
Multi-step reaction with 2 steps
1: pyridinium chlorochromate; magnesium sulfate / chloroform / 3 h / Sealed tube
2: hydroxylamine hydrochloride; sodium acetate / water; ethanol; tetrahydrofuran / 72 h / 20 °C
With hydroxylamine hydrochloride; sodium acetate; magnesium sulfate; pyridinium chlorochromate; In tetrahydrofuran; ethanol; chloroform; water;
DOI:10.1016/j.tetlet.2015.12.038
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