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Merck

442003

Sigma-Aldrich

反式-2-丁烯醛二乙基缩醛

technical, 90%

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About This Item

线性分子式:
CH3CH=CHCH(OC2H5)2
CAS号:
分子量:
144.21
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

等级

technical

方案

90%

折射率

n20/D 1.412 (lit.)

沸点

146-150 °C (lit.)

密度

0.831 g/mL at 25 °C (lit.)

SMILES字符串

[H]\C(C)=C(\[H])C(OCC)OCC

InChI

1S/C8H16O2/c1-4-7-8(9-5-2)10-6-3/h4,7-8H,5-6H2,1-3H3/b7-4+

InChI key

ZUMISMXLQDKQDS-QPJJXVBHSA-N

一般描述

trans-2-Butenal diethyl acetal is an acetal. Acetals are usually derived from the aldehydes. They have two single-bonded oxygen atoms attached to the same carbon atom. They are stable under basic conditions and they can be hydrolyzed back to the carbonyl compound. Acetals serves as a carbonyl protecting group and also are present as functional groups in glycosidic bonds. trans-2-Butenal diethyl acetal has been synthesized from trans-2-butenal with ethanol in the presence of methanesulfonic acid or methylsulfonate as catalysts.[1]

应用

trans-2-Butenal diethyl acetal may be used in the preparation of 2S,3S-epoxybutan-1-ol, an intermediate in the synthesis of erythromycin antibiotic.[2]

象形图

FlameExclamation mark

警示用语:

Warning

危险分类

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

93.2 °F - closed cup

闪点(°C)

34 °C - closed cup

个人防护装备

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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An Efficient Method for One-Pot Reductive Cleavage of Acetals to Primary Alcohols Using a Bimetal Redox Couple CoCl2. 6H2O-Zn.
Sarma K and Goswami A.
Letters in Organic Chemistry, 6(7), 568-572 (2009)
SYNTHESIS OF trans-2-BUTENAL DIETHYL ACETAL CATALYZED BY METHYLSUFONIC ACID OR METHYLSULFONATE [J].
Lifang Z, et al.
Speciality Petrochemicals, 3, 008-008 (2006)

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