397261
N-(2-Aminoethyl)acetamide
technical grade, 90%
Synonym(s):
N-Acetylethylenediamine
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About This Item
Linear Formula:
CH3C(O)NHCH2CH2NH2
CAS Number:
Molecular Weight:
102.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1743120
Product Name
N-(2-Aminoethyl)acetamide, technical grade, 90%
InChI
1S/C4H10N2O/c1-4(7)6-3-2-5/h2-3,5H2,1H3,(H,6,7)
SMILES string
CC(=O)NCCN
InChI key
DAKZISABEDGGSV-UHFFFAOYSA-N
grade
technical grade
assay
90%
refractive index
n20/D 1.485 (lit.)
bp
128 °C/3 mmHg (lit.)
mp
50 °C (lit.)
density
1.066 g/mL at 25 °C (lit.)
functional group
amide
amine
Quality Level
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Application
N-(2-Aminoethyl)acetamide may be used in the preparation of mixed two-component monolayers on glassy carbon. It may be used in the synthesis of lysidine.
General description
N-(2-Aminoethyl)acetamide is an organic building block.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>230.0 °F - closed cup
flash_point_c
> 110 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
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Enrique Huang Kwan et al.
Dalton transactions (Cambridge, England : 2003), 45(40), 15931-15941 (2016-07-08)
A new long-tethered boron-containing (P-B-P)-pincer ligand 8 has been synthesized. Complexation of 8 with [Ir(coe)
Emma J Wright et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(19), 5550-5554 (2014-04-12)
Mixed two-component monolayers on glassy carbon are prepared by electrochemical oxidation of N-(2-aminoethyl)acetamide and mono-N-Boc-hexamethylenediamine in mixed solution. Subsequent N-deprotection, amide coupling and solid-phase synthetic steps lead to electrode-surface functionalisation with maleimide, with controlled partial coverage of this cysteine-binding group
The Mechanism of Acid Hydrolysis of Lysidine and N-(2-Aminotheyl) acetamide and Related Amides.
Haake P and Watson J.
The Journal of Organic Chemistry, 35(12), 4063-4067 (1970)
Yoonkyung Kim et al.
Purinergic signalling, 5(1), 39-50 (2008-07-05)
As a continued effort to develop multivalent ligands to enhance the pharmacological effects of monomeric drugs, DITC-APEC, a chemically reactive nucleoside A(2A) adenosine receptor (AR) agonist, was employed to derivatize the surface of third-generation (G3) polyamidoamine (PAMAM) dendrimers. The resulting
Ling Li et al.
Molecular cell, 80(3), 525-540 (2020-10-18)
Well-balanced and timed metabolism is essential for making a high-quality egg. However, the metabolic framework that supports oocyte development remains poorly understood. Here, we obtained the temporal metabolome profiles of mouse oocytes during in vivo maturation by isolating large number of
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