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1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE

Base Information Edit
  • Chemical Name:1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE
  • CAS No.:288573-56-8
  • Molecular Formula:C16H23 F N2 O2
  • Molecular Weight:294.369
  • Hs Code.:
  • Mol file:288573-56-8.mol
1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE

Synonyms:1-tert-Butoxycarbonyl-4-[(4-fluorophenyl)amino]piperidine;4-(4-Fluorophenylamino)piperidine-1-carboxylic acid tert-butyl ester;tert-Butyl 4-(4-fluoroanilino)-1-piperidinecarboxylate

 This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE Edit
Chemical Property:
  • Boiling Point:400.4±40.0 °C(Predicted) 
  • PKA:5.09±0.20(Predicted) 
  • PSA:41.57000 
  • Density:1.159±0.06 g/cm3(Predicted) 
  • LogP:3.64800 
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Uses 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE is a heterocyclic derivative and can be used as a pharmaceutical intermediate.
Technology Process of 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE

There total 6 articles about 1-BOC-4-(4-FLUORO-PHENYLAMINO)-PIPERIDINE 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 sodium cyanoborohydride; acetic acid; In dichloromethane; at 0 - 20 ℃; for 15h;
Guidance literature:
With tris-(dibenzylideneacetone)dipalladium(0); DavePhos; In 5,5-dimethyl-1,3-cyclohexadiene; at 140 ℃; for 4h; Inert atmosphere;
Guidance literature:
With sodium tris(acetoxy)borohydride; In dichloromethane; at 20 ℃; for 18h;
DOI:10.1016/S0968-0896(00)00077-8
Refernces Edit