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Merck
CN

47675

Sigma-Aldrich

二乙醇缩甲醛

absolute, over molecular sieve (H2O ≤0.01%), ≥99.0% (GC)

别名:

二乙氧基甲烷, 甲醛缩二乙醇

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About This Item

线性分子式:
CH2(OC2H5)2
CAS号:
分子量:
104.15
Beilstein:
1697253
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案:
≥99.0% (GC)
沸点:
87-88 °C (lit.)
蒸汽压:
60 mmHg ( 25 °C)

蒸汽密度

3.6 (vs air)

质量水平

蒸汽压

60 mmHg ( 25 °C)

等级

absolute

方案

≥99.0% (GC)

表单

liquid

自燃温度

346 °F

质量

over molecular sieve (H2O ≤0.01%)

折射率

n20/D 1.373 (lit.)
n20/D 1.374

沸点

87-88 °C (lit.)

密度

0.831 g/mL at 25 °C (lit.)

官能团

ether

SMILES字符串

CCOCOCC

InChI

1S/C5H12O2/c1-3-6-5-7-4-2/h3-5H2,1-2H3

InChI key

KLKFAASOGCDTDT-UHFFFAOYSA-N

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一般描述

Formaldehyde diethyl acetal (FDEA, diethoxymethane, DEM) is a diethyl acetal. It has been synthesized from ethanol and aqueous formaldehyde. It is a low boiling solvent useful for sodium hydride reactions, organolithium chemistry, copper-catalyzed conjugate additions and phase-transfer reactions. It is a potential alternate for tetrahydrofuran, dichloromethane, glyme and methylal. DEM is an ethoxymethylating agent, a formaldehyde equivalent and a carbonylation substrate. Its condensation with 2-propylresorcinol to form resorcin[n]arenes (n=4–7) has been investigated. The IR and Raman spectra and conformations of DEM have been studied. NMR spectroscopy has been used to study the aggregation behavior of organolithium compounds in diethoxymethane. Unimolecular metastable decomposition of DEM upon electron impact has been studied. Solubility of non-polar gases in DEM has been evaluated.

应用

Formaldehyde diethyl acetal may be used as a solvent in the esterification of carboxylic acids and in the O-alkylation of a variety of phenols.

象形图

Flame

警示用语:

Danger

危险声明

危险分类

Flam. Liq. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 1

闪点(°F)

23.0 °F - closed cup

闪点(°C)

-5 °C - closed cup

个人防护装备

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

法规信息

危险化学品

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分析证书(COA)

Lot/Batch Number

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访问文档库

NMR spectroscopy of organolithium compounds, Part XVI: The aggregation behavior of butyllithium, phenyllithium, and lithium diisopropylamide in dimethoxy-and diethoxymethane.
Bergander K, et al.
Tetrahedron, 50(20), 5861-5868 (1994)
Use of Diethoxymethane as a Solvent for Phase-Transfer Esterification of Carboxylic Acids.
Coleman MT.
Synthetic Communications, 42(13), 1911-1913 (2012)
Sc(OTf)3-catalyzed cyclocondensation of 2-propylresorcinol with diethoxymethane. Formation and fragmentation of resorcin [n] arenes.
Morikawa O, et al.
Tetrahedron Letters, 45(29), 5731-5734 (2004)
Solubility of non polar gases in formaldehyde diethyl acetal between-10 and 30?C, and 1 Atm partial pressure of gas.
Lizano LP, et al.
Journal of Solution Chemistry, 19(7), 721-728 (1990)
Metastable decompositions of gem-dialkoxyalkanes upon electron impact. III. Diethoxymethane (CH2 (OCH2CH3)2).
Tajima S, et al.
Rapid Communications in Mass Spectrometry, 14(14), 1195-1199 (2000)

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