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2-Phenylcyclohexanone oxime

Base Information
  • Chemical Name:2-Phenylcyclohexanone oxime
  • CAS No.:22591-17-9
  • Molecular Formula:C12H15 N O
  • Molecular Weight:189.257
  • Hs Code.:2928000090
  • NSC Number:122965
  • DSSTox Substance ID:DTXSID20421056
  • Nikkaji Number:J83.196D
  • Mol file:22591-17-9.mol
2-Phenylcyclohexanone oxime

Synonyms:2-phenylcyclohexanone oxime;22591-17-9;NSC122965;(NZ)-N-(2-phenylcyclohexylidene)hydroxylamine;DTXSID20421056;AKOS024324806;NSC-122965

Suppliers and Price of 2-Phenylcyclohexanone oxime
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
  • Sigma-Aldrich
  • 2-PHENYLCYCLOHEXANONE OXIME Aldrich
  • 1ea
  • $ 57.00
  • American Custom Chemicals Corporation
  • 2-PHENYLCYCLOHEXANONE OXIME 95.00%
  • 5MG
  • $ 504.47
Total 2 raw suppliers
Chemical Property of 2-Phenylcyclohexanone oxime
Chemical Property:
  • Vapor Pressure:3.48E-05mmHg at 25°C 
  • Boiling Point:339.8°C at 760 mmHg 
  • Flash Point:210.7°C 
  • PSA:32.59000 
  • Density:1.1g/cm3 
  • LogP:3.17440 
  • XLogP3:2.9
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:1
  • Exact Mass:189.115364102
  • Heavy Atom Count:14
  • Complexity:206
Purity/Quality:

2-PHENYLCYCLOHEXANONE OXIME Aldrich *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CCC(=NO)C(C1)C2=CC=CC=C2
  • Isomeric SMILES:C1CC/C(=N/O)/C(C1)C2=CC=CC=C2
Technology Process of 2-Phenylcyclohexanone oxime

There total 5 articles about 2-Phenylcyclohexanone oxime 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 acetate; In methanol; water; at 60 ℃;
DOI:10.1021/jo00128a009
Guidance literature:
With potassium carbonate; In ethanol; water;
Guidance literature:
Multi-step reaction with 2 steps
1: palladium diacetate; tris-(o-tolyl)phosphine; sodium acetate; pyrrolidine; tert-Octylamine / 1,4-dioxane / 110 °C / Inert atmosphere; Schlenk technique; Sealed tube
2: sodium hydroxide; hydroxylamine hydrochloride / ethanol; water / 20 °C / Inert atmosphere; Schlenk technique
With pyrrolidine; tert-Octylamine; hydroxylamine hydrochloride; sodium acetate; palladium diacetate; tris-(o-tolyl)phosphine; sodium hydroxide; In 1,4-dioxane; ethanol; water;
DOI:10.1002/cjoc.201800206
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