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1-Phenylpiperidin-3-one

Base Information Edit
  • Chemical Name:1-Phenylpiperidin-3-one
  • CAS No.:148494-90-0
  • Molecular Formula:C11H13 N O
  • Molecular Weight:175.23
  • Hs Code.:2933399090
  • Mol file:148494-90-0.mol
1-Phenylpiperidin-3-one

Synonyms:1-Phenyl-3-piperidinone

Suppliers and Price of 1-Phenylpiperidin-3-one
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
  • 1-Phenylpiperidin-3-one
  • 250mg
  • $ 205.00
  • Medical Isotopes, Inc.
  • 1-Phenylpiperidin-3-one
  • 2.5 g
  • $ 2480.00
  • American Custom Chemicals Corporation
  • 1-PHENYLPIPERIDIN-3-ONE 95.00%
  • 5MG
  • $ 498.99
  • Alichem
  • 1-Phenylpiperidin-3-one
  • 25g
  • $ 4168.89
  • Alichem
  • 1-Phenylpiperidin-3-one
  • 10g
  • $ 2255.22
  • Alichem
  • 1-Phenylpiperidin-3-one
  • 5g
  • $ 2229.12
  • Acrotein
  • 1-Phenylpiperidin-3-one 97%
  • 1g
  • $ 440.92
  • Acrotein
  • 1-Phenylpiperidin-3-one 97%
  • 0.25g
  • $ 176.37
Total 24 raw suppliers
Chemical Property of 1-Phenylpiperidin-3-one Edit
Chemical Property:
  • Vapor Pressure:0.001mmHg at 25°C 
  • Boiling Point:313 ºC 
  • Flash Point:124 ºC 
  • PSA:20.31000 
  • Density:1.107 
  • LogP:1.92090 
  • Storage Temp.:2-8°C 
Purity/Quality:

98%min *data from raw suppliers

1-Phenylpiperidin-3-one *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses 1-Phenylpiperidin-3-one is used in the synthetic preparation of lipoxygenase inhibition structure.
Technology Process of 1-Phenylpiperidin-3-one

There total 7 articles about 1-Phenylpiperidin-3-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:
Guidance literature:
With hydrogenchloride; In tert-butyl methyl ether; water; for 168h;
DOI:10.1021/acs.orglett.7b00344
Guidance literature:
Multi-step reaction with 3 steps
1: methanesulfonic acid / 20 - 50 °C
2: tri tert-butylphosphoniumtetrafluoroborate; bis(dibenzylideneacetone)-palladium(0); potassium tert-butylate / toluene / 24 h / 100 °C / Schlenk technique
3: hydrogenchloride / water; tert-butyl methyl ether / 168 h
With hydrogenchloride; methanesulfonic acid; potassium tert-butylate; bis(dibenzylideneacetone)-palladium(0); tri tert-butylphosphoniumtetrafluoroborate; In tert-butyl methyl ether; water; toluene;
DOI:10.1021/acs.orglett.7b00344
Guidance literature:
Multi-step reaction with 2 steps
1: tri tert-butylphosphoniumtetrafluoroborate; bis(dibenzylideneacetone)-palladium(0); potassium tert-butylate / toluene / 24 h / 100 °C / Schlenk technique
2: hydrogenchloride / water; tert-butyl methyl ether / 168 h
With hydrogenchloride; potassium tert-butylate; bis(dibenzylideneacetone)-palladium(0); tri tert-butylphosphoniumtetrafluoroborate; In tert-butyl methyl ether; water; toluene;
DOI:10.1021/acs.orglett.7b00344
Refernces Edit
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