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Merck
CN

D157805

Sigma-Aldrich

N,N′-二甲基乙二胺

98%

别名:

DMEDA, 1,2-双(甲氨基)乙烷

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About This Item

线性分子式:
CH3NHCH2CH2NHCH3
CAS号:
分子量:
88.15
Beilstein:
878142
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

形式

liquid

折射率

n20/D 1.431 (lit.)

bp

119 °C (lit.)

密度

0.819 g/mL at 20 °C (lit.)

SMILES字符串

CNCCNC

InChI

1S/C4H12N2/c1-5-3-4-6-2/h5-6H,3-4H2,1-2H3

InChI key

KVKFRMCSXWQSNT-UHFFFAOYSA-N

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应用

N,N′-二甲基乙二胺可用作以下过程的配体:
  • 铜催化铁氰化钾参与的芳基溴代物的氰化反应,形成相应的苄腈。
  • 铜催化碳化二亚胺和异氰基乙酸酯的串联反应,形成苯并咪唑[1,5-α]咪唑。
  • 1,1-二溴烯烃的氨基硫化反应,形成N-稠杂环。
  • 与氯化亚铁结合,用于NH-亚砜亚胺与芳基碘化物的N-芳基化反应,形成N-芳基亚砜亚胺。
  • 丁醇钾存在下,它可催化未活化苯的直接C-H芳基化反应,形成相应的联芳基。

象形图

FlameCorrosion

警示用语:

Danger

危险声明

危险分类

Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

WGK

WGK 3

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

危险化学品

分析证书(COA)

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Ghotas Evindar et al.
The Journal of organic chemistry, 71(5), 1802-1808 (2006-02-25)
A general method for the formation of benzoxazoles via a copper-catalyzed cyclization of ortho-haloanilides is reported. This approach complements the more commonly used strategies for benzoxazole formation which require 2-aminophenols as substrates. The reaction involves an intramolecular C-O cross-coupling of
Kim A Lennox et al.
Oligonucleotides, 16(1), 26-42 (2006-04-06)
A wide variety of modified oligonucleotides have been tested as antisense agents. Each chemical modification produces a distinct profile of potency, toxicity, and specificity. Novel cationic phosphoramidate-modified antisense oligonucleotides have been developed recently that have unique and interesting properties. We
An environmentally benign procedure for the Cu-catalyzed cyanation of aryl bromides.
Schareina T, et al.
Tetrahedron Letters, 46(15), 2585-2588 (2005)
Iron?Catalyzed C N Cross?Coupling of Sulfoximines with Aryl Iodides.
Correa A, et al.
Advanced Synthesis & Catalysis, 350(3), 391-394 (2008)
Copper-catalyzed synthesis of N-fused heterocycles through regioselective 1, 2-aminothiolation of 1, 1-dibromoalkenes.
Xu H, et al.
Organic Letters, 12(16), 3704-3707 (2010)

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