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Merck
CN

370460

Sigma-Aldrich

二乙氧基乙腈

97%

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About This Item

线性分子式:
(C2H5O)2CHCN
CAS号:
分子量:
129.16
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

形式

liquid

折射率

n20/D 1.4 (lit.)

bp

167.7 °C/773 mmHg (lit.)

mp

−19-−18 °C (lit.)

密度

0.929 g/mL at 25 °C (lit.)

SMILES字符串

CCOC(OCC)C#N

InChI

1S/C6H11NO2/c1-3-8-6(5-7)9-4-2/h6H,3-4H2,1-2H3

InChI key

UDELMRIGXNCYLU-UHFFFAOYSA-N

一般描述

Diethoxyacetonitrile is a 2,2-dialkoxyalkanenitrile derivative. Reaction of hydrocyanic acid with various ortho esters of aliphatic and aromatic acids in the presence of acidic catalyst has been reported to afford diethoxyacetonitrile. Houben-Hoesch reaction of diethoxyacetonitrile with 1,2,4-trimethoxybenzene affords tris(2,4,5-trimethoxyphenyl)methane.

应用

Diethoxyacetonitrile may be used in the preparation of methyl 5-diethoxymethylimidazole-4-carboxylate, via anionic cycloaddition reaction with methyl isocyanoacetate.

象形图

FlameExclamation mark

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Flam. Liq. 3

WGK

WGK 3

闪点(°F)

120.2 °F

闪点(°C)

49 °C

个人防护装备

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

法规信息

危险化学品

分析证书(COA)

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An efficient synthesis of 5-diethoxymethylimidazole-4-carboxylate, a potential precursor for various imidazole derivatives.
Murakami T, et al.
Tetrahedron Letters, 23(45), 4729-4732 (1982)
2, 2-Dialkoxyalkanenitriles.
Erickson JG.
Journal of the American Chemical Society, 73(3), 1338-1339 (1951)
An anomalous Houben-Hoesch reaction and some applications in arylation reactions.
Sanchez-Viesca F, et al.
Organic Prep. and Proc. Int., 36(2), 135-140 (2004)

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