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tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate

Base Information
  • Chemical Name:tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate
  • CAS No.:127828-22-2
  • Molecular Formula:C9H20 N2 O3
  • Molecular Weight:204.269
  • Hs Code.:2924199090
  • European Community (EC) Number:821-336-1
  • DSSTox Substance ID:DTXSID40477696
  • Nikkaji Number:J2.297.386J
  • Wikidata:Q72510743
  • Mol file:127828-22-2.mol
tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate

Synonyms:127828-22-2;tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate;t-Boc-N-amido-PEG1-Amine;Amino-PEG2-NH-Boc;tert-butyl N-[2-(2-aminoethoxy)ethyl]carbamate;N-Boc-2-(2-aminoethoxy)ethylamine;BocNH-PEG1-CH2CH2NH2;tert-Butyl [2-(2-aminoethoxy)ethyl]carbamate;MFCD12031501;N-Boc-2-(2-amino-ethoxy)ethylamine;N-Boc-2-(2-amino-ethoxy)-ethylamine;tert-butyl 2-(2-aminoethoxy)ethylcarbamate;Carbamic acid, N-[2-(2-aminoethoxy)ethyl]-, 1,1-dimethylethyl ester;N-(tert-Butoxycarbonyl)-2-(2-aminoethoxy)ethylamine;Carbamic acid, [2-(2-aminoethoxy)ethyl]-, 1,1-dimethylethyl ester (9CI);t-Boc-N-amido-PEG-amine, MW 1,000;SCHEMBL222081;DTXSID40477696;VULKFBHOEKTQSF-UHFFFAOYSA-N;N-Boc-2-(2-Aminoethoxy)ethanamine;Carbamic acid, [2-(2-aminoethoxy)ethyl]-, 1,1-dimethylethyl ester;AKOS013065977;CS-W008279;HY-W008279;N-Boc-2-aminoethyl 2-aminoethyl ether;t-Boc-N-amido-PEG-amine, MW 2,000;t-Boc-N-amido-PEG-amine, MW 3,400;t-Boc-N-amido-PEG-amine, MW 5,000;BP-22862;BP-23695;BP-23696;BP-23697;BP-25687;BP-25688;BP-28677;SY065871;tertbutyl 2-(2-aminoethoxy)ethylcarbamate;t-Boc-N-amido-PEG-amine, MW 10,000;t-butyl-(2-(2-aminoethoxy)ethyl)carbamate;tert-butyl 2-(2-aminoethoxyl)ethylcarbamate;B5683;n-t-butoxycarbonyl-3-oxa-1,5-pentanediamine;tert-Butyl(2-(2-aminoethoxy)ethyl)carbamate;2-{2-(t-butoxycarbonylamino)ethoxy}ethylamine;EN300-316617;H10185;A889144;N-(tert-butyloxycarbonyl)-2,2'-oxybis(ethylamine);[2-(2-Aminoethoxy)ethyl]carbamic Acid tert-Butyl Ester;1-(2-(tert-butyloxycarbonylamino)ethoxy)-2-aminoethane

Suppliers and Price of tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate
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
  • tert-Butyl(2-(2-aminoethoxy)ethyl)carbamate
  • 100mg
  • $ 65.00
  • TCI Chemical
  • N-(tert-Butoxycarbonyl)-2-(2-aminoethoxy)ethylamine >98.0%(GC)(T)
  • 1g
  • $ 154.00
  • TCI Chemical
  • N-(tert-Butoxycarbonyl)-2-(2-aminoethoxy)ethylamine >98.0%(GC)(T)
  • 200mg
  • $ 52.00
  • SynQuest Laboratories
  • tert-Butyl [2-(2-aminoethoxy)ethyl]carbamate
  • 250 mg
  • $ 77.00
  • SynQuest Laboratories
  • tert-Butyl [2-(2-aminoethoxy)ethyl]carbamate
  • 1 g
  • $ 189.00
  • SynQuest Laboratories
  • tert-Butyl [2-(2-aminoethoxy)ethyl]carbamate
  • 5 g
  • $ 704.00
  • purepeg
  • tert-butylN-<2-(2-aminoethoxy)ethyl>carbamate min.97%
  • 5 g
  • $ 479.00
  • purepeg
  • tert-butylN-<2-(2-aminoethoxy)ethyl>carbamate min.97%
  • 1 g
  • $ 134.00
  • Iris Biotech GmbH
  • Boc-NH-ethoxy-ethylamine
  • 1 g
  • $ 132.30
  • Iris Biotech GmbH
  • Boc-NH-ethoxy-ethylamine
  • 5 g
  • $ 472.50
Total 50 raw suppliers
Chemical Property of tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Refractive Index:1.457 
  • Boiling Point:321.128°C at 760 mmHg 
  • PKA:12.24±0.46(Predicted) 
  • Flash Point:148.013°C 
  • PSA:77.07000 
  • Density:1.024g/cm3 
  • LogP:1.39110 
  • Storage Temp.:2-8°C(protect from light) 
  • XLogP3:-0.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:204.14739250
  • Heavy Atom Count:14
  • Complexity:166
Purity/Quality:

99%, *data from raw suppliers

tert-Butyl(2-(2-aminoethoxy)ethyl)carbamate *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)(C)OC(=O)NCCOCCN
  • Description t-Boc-N-Amido-PEG1-amine is a small molecule PEG reagent containing an amino group and Boc-protected amino group. The amino group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Technology Process of tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate

There total 10 articles about tert-Butyl (2-(2-aminoethoxy)ethyl)carbamate 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 palladium 10% on activated carbon; hydrogen; In methanol; at 25 ℃; for 8h;
DOI:10.1016/j.ejmech.2016.04.001
Guidance literature:
With sodium hydroxide; In tetrahydrofuran; methanol; at 20 ℃;
DOI:10.1016/j.tetlet.2006.02.119
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