N-Boc-ethylenediamine

Synonym
Product Category
Product Code
CAS Number
MDL Number
Pubchem CID
Reaxys RN
N-Boc-1,2-diaminoethane, tert-Butyl N-(2-aminoethyl)carbamate
Non-Fluorochemicals, API & Intermediates
KUMI0F984
57260-73-8

PubChem ID

Reax
MFCD00191871

PubChem ID
187201
1932330
image-155171-Trimethyl(trifluoromethyl)silane_reagent.png
Chemical Name
Molecular Formula
Molecular Weight
Assay
Appearance
Boiling Point
Packaging
Storage
N-Boc-ethylenediamine
C7H16N2O2
160.21
≥98%
Colorless to Light Yellow Liquid
70-73°C
10g,25g,50g,100g,250g,500g,1kg and 25kg
Store at room temperature
N-Boc-ethylenediamine (also known as N-Boc-1,2-diaminoethane, tert-Butyl N-(2-aminoethyl)carbamate) is typically in the preparation of thyronamine derivatives. It is also used more in both oligonucleotides and peptide synthesis.
A convenient and scalable synthesis of ethyl N-[(2-Boc-amino)ethyl]glycinate and its hydrochloride. Key intermediates for peptide nucleic acid synthesis. [1]
Symmetrical 1,3-dicarbonyl biscatecholamide ligands as sequestering agents for uranyl decorporation. [2]
Design, characterization and in vitro evaluation of novel shell crosslinked poly(butylene adipate)-co-N-succinyl chitosan nanogels containing loteprednol etabonate: A new system for therapeutic effect enhancement via controlled drug delivery. [3]
References:
[1] R.D.Viirre, et al, J. Org. Chem., 2003, 68(14), pp 1630-1632.
[2] Q.Zhang, et al, Polyhedron, 2015, 87, pp 417-423.
[3] F.H.Nasr, et al, Eur. J. Med. Chem., 2015, 102, pp 132-142.
Signal Word
Hazard Statements
Precautionary Statements
HS Code
RIDADR
Legal Information
Danger
H314
P280,P301+P330+P331,P303+P361+P353,P304+P340+P310,P305+P351+P338,P363
29241900
UN 2735 8/PG III

1. Product Specification
2. Safety Data Sheet
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