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Merck
CN

A24001

Sigma-Aldrich

丙烯醛缩二乙醇

96%

别名:

3,3-二乙氧基丙烯

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About This Item

线性分子式:
CH2=CHCH(OCH2CH3)2
CAS号:
分子量:
130.18
Beilstein:
1701567
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

96%

表单

liquid

折射率

n20/D 1.398 (lit.)

沸点

125 °C (lit.)

密度

0.854 g/mL at 25 °C (lit.)

SMILES字符串

CCOC(OCC)C=C

InChI

1S/C7H14O2/c1-4-7(8-5-2)9-6-3/h4,7H,1,5-6H2,2-3H3

InChI key

MCIPQLOKVXSHTD-UHFFFAOYSA-N

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应用

丙烯醛二乙基缩醛广泛用于进行化学选择性 Heck 芳基化,合成 3-芳基丙酸酯或肉桂醛衍生物。

它也可用作合成天然产物如 (-)-(Z)-脱氧普卡灵、(-)-Laulimalide、botryodiplodin、neolaulimalide 和 isolaulimalide 的前体之一。

象形图

FlameExclamation mark

警示用语:

Danger

危险声明

预防措施声明

危险分类

Eye Irrit. 2 - Flam. Liq. 2

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

59.0 °F - closed cup

闪点(°C)

15 °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

从最新的版本中选择一种:

分析证书(COA)

Lot/Batch Number

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如果您需要特殊版本,可通过批号或批次号查找具体证书。

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Synthesis of (?)-and (−)-botryodiplodin using stereoselective radical cyclizations of acyclic esters and acetals.
Nouguier R et al.
Tetrahedron Asymmetry, 14(19), 3005-3018 (2003)
Stefano Parisotto et al.
Organic & biomolecular chemistry, 15(4), 884-893 (2017-01-04)
As part of our ongoing work on the synthesis of a new class of plant hormones named Strigolactones (SLs) and their analogues, we became interested in tracing bioactive molecules with red emitting BODIPY fluorophores in order to unravel signaling and
Mohammad Saidur Rhaman et al.
Plant & cell physiology, 61(5), 967-977 (2020-03-08)
Myrosinase (β-thioglucoside glucohydrolase, enzyme nomenclature, EC 3.2.1.147, TGG) is a highly abundant protein in Arabidopsis guard cells, of which TGG1 and TGG2 function redundantly in abscisic acid (ABA)- and methyl jasmonate-induced stomatal closure. Reactive carbonyl species (RCS) are α,β-unsaturated aldehydes
An efficient palladium-catalyzed synthesis of cinnamaldehydes from acrolein diethyl acetal and aryl iodides and bromides.
Battistuzzi G, et al.
Organic Letters, 5(5), 777-780 (2003)
Total synthesis of neolaulimalide and isolaulimalide.
Gollner A and Mulzer J.
Organic Letters, 10(20), 4701-4704 (2008)

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