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About This Item
线性分子式:
CH3C(O)NHCH2CH2NH2
CAS号:
分子量:
102.14
Beilstein:
1743120
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
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等級
technical grade
化驗
90%
折射率
n20/D 1.485 (lit.)
bp
128 °C/3 mmHg (lit.)
mp
50 °C (lit.)
密度
1.066 g/mL at 25 °C (lit.)
官能基
amide
amine
SMILES 字串
CC(=O)NCCN
InChI
1S/C4H10N2O/c1-4(7)6-3-2-5/h2-3,5H2,1H3,(H,6,7)
InChI 密鑰
DAKZISABEDGGSV-UHFFFAOYSA-N
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一般說明
N-(2-Aminoethyl)acetamide is an organic building block.
應用
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.
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
>230.0 °F - closed cup
閃點（°C）
> 110 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type N95 (US)
其他客户在看
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
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
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)
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