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4-(2-Boc-aminoethyl)piperidine

Base Information
  • Chemical Name:4-(2-Boc-aminoethyl)piperidine
  • CAS No.:165528-81-4
  • Molecular Formula:C12H24N2O2
  • Molecular Weight:228.335
  • Hs Code.:2933399090
  • European Community (EC) Number:688-374-7
  • DSSTox Substance ID:DTXSID10363537
  • Nikkaji Number:J2.348.862K
  • Wikidata:Q72448089
  • ChEMBL ID:CHEMBL4525509
  • Mol file:165528-81-4.mol
4-(2-Boc-aminoethyl)piperidine

Synonyms:165528-81-4;4-(2-BOC-AMINOETHYL)PIPERIDINE;4-[2-(Boc-amino)ethyl]piperidine;tert-butyl (2-(piperidin-4-yl)ethyl)carbamate;(2-Piperidin-4-yl-ethyl)-carbamic acid tert-butyl ester;tert-butyl N-(2-piperidin-4-ylethyl)carbamate;tert-butyl N-[2-(piperidin-4-yl)ethyl]carbamate;tert-butyl 2-(piperidin-4-yl)ethylcarbamate;MFCD01318373;Carbamic acid, [2-(4-piperidinyl)ethyl]-, 1,1-dimethylethyl ester;Carbamic acid, N-[2-(4-piperidinyl)ethyl]-, 1,1-dimethylethyl ester;tert-butyl (2-piperidin-4-ylethyl)carbamate;SCHEMBL346052;CHEMBL4525509;DTXSID10363537;CS-B0446;AKOS000160613;PS-4227;SB43150;AC-24270;BL000877;SY023589;tert-butyl 2-piperidin-4-ylethylcarbamate;BB 0262509;FT-0648147;4-(2-Boc-aminoethyl) piperidine, AldrichCPR;4-(2-tert-Butoxycarbonylaminoethyl)piperidine;EN300-76331;tert-butyl(2-(piperidin-4-yl)ethyl)carbamate;4-(2-tert-butoxycarbonylaminoethyl)-piperidine;N-(tert-Butoxycarbonyl)piperidine-4-ethaneamine;tert-Butyl 2-(piperidin-4-yl)(ethyl)carbamate;N-t-butoxycarbonyl 2-(piperidin-4-yl)-ethylamine;Q-102973;1,1-dimethylethyl [2-(4-piperidinyl)ethyl]carbamate;(2-Piperidin-4-ylethyl) carbamic acid tert-butyl ester;N-[2-(4-piperidinyl)ethyl]-carbamic acid tert-butyl ester

Suppliers and Price of 4-(2-Boc-aminoethyl)piperidine
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
  • TRC
  • 4-(2-Boc-aminoethyl)piperidine
  • 500mg
  • $ 105.00
  • TRC
  • 4-(2-Boc-aminoethyl)piperidine
  • 100mg
  • $ 45.00
  • SynChem
  • TERT-BUTYL 2-(PIPERIDIN-4-YL)ETHYLCARBAMATE 95%
  • 1 g
  • $ 115.00
  • Matrix Scientific
  • tert-Butyl (2-(piperidin-4-yl)ethyl)carbamate 95%
  • 500mg
  • $ 217.00
  • Matrix Scientific
  • tert-Butyl (2-(piperidin-4-yl)ethyl)carbamate 95%
  • 5g
  • $ 1055.00
  • Matrix Scientific
  • tert-Butyl (2-(piperidin-4-yl)ethyl)carbamate 95%
  • 1g
  • $ 349.00
  • Crysdot
  • 4-(2-Boc-aminoethyl)piperidine 95+%
  • 5g
  • $ 290.00
  • Chemenu
  • tert-butyl2-(piperidin-4-yl)ethylcarbamate 95%
  • 5g
  • $ 241.00
  • Biosynth Carbosynth
  • 4-(2-Boc-aminoethyl)piperidine
  • 5 g
  • $ 325.00
  • Biosynth Carbosynth
  • 4-(2-Boc-aminoethyl)piperidine
  • 10 g
  • $ 600.00
Total 54 raw suppliers
Chemical Property of 4-(2-Boc-aminoethyl)piperidine
Chemical Property:
  • Vapor Pressure:0.000106mmHg at 25°C 
  • Refractive Index:1.459 
  • Boiling Point:337.3 °C at 760 mmHg 
  • PKA:12.86±0.46(Predicted) 
  • Flash Point:157.8 °C 
  • PSA:50.36000 
  • Density:0.971 g/cm3 
  • LogP:2.62050 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2–8 °C 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:5
  • Exact Mass:228.183778013
  • Heavy Atom Count:16
  • Complexity:218
Purity/Quality:

97% *data from raw suppliers

4-(2-Boc-aminoethyl)piperidine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NCCC1CCNCC1
Technology Process of 4-(2-Boc-aminoethyl)piperidine

There total 1 articles about 4-(2-Boc-aminoethyl)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:
Multi-step reaction with 3 steps
1: 46.9 g / ammonium chloride / H2O; methanol / Heating
2: 2-methyl-propan-2-ol / 12 h / 20 °C
3: 21.9 g / H2; AcOH / PtO2 / 96 h / 35 °C
With ammonium chloride; hydrogen; acetic acid; platinum(IV) oxide; In methanol; water; tert-butyl alcohol;
DOI:10.1021/jm051272l
Guidance literature:
With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In N,N-dimethyl-formamide; at 25 ℃; for 3h; Inert atmosphere;
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