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Merck
CN

310778

Sigma-Aldrich

3,4-二乙氧基-3-环丁烯-1,2-二酮

98%

别名:

四方酸二乙酯, 方酸二乙酯

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About This Item

线性分子式:
(C2H5O)2C4(=O)2
CAS号:
分子量:
170.16
Beilstein:
640626
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

表单

liquid

折射率

n20/D 1.509 (lit.)

沸点

95 °C/0.1 mmHg (lit.)

密度

1.15 g/mL at 25 °C (lit.)

官能团

ether
ketone

SMILES字符串

CCOC1=C(OCC)C(=O)C1=O

InChI

1S/C8H10O4/c1-3-11-7-5(9)6(10)8(7)12-4-2/h3-4H2,1-2H3

InChI key

DFSFLZCLKYZYRD-UHFFFAOYSA-N

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一般描述

3,4-二乙氧基-3-环丁烯-1,2-二酮(方酸二乙酯)与糖胺(通过还原低聚糖形成)的反应已被研究。所形成的衍生物与氨基官能化的脂质、固体或蛋白相连。

应用

3,4-二乙氧基-3-环丁烯-1,2-二酮可用作合成呋喃酮和醌的起始材料。它会经过胺和不饱和有机硅烷的乙氧基取代。

象形图

Health hazardExclamation mark

警示用语:

Danger

危险分类

Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

230.0 °F - closed cup

闪点(°C)

110 °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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Organic Syntheses, 69, 220-220 (1990)
Journal of the Chemical Society. Perkin Transactions 1, 263-263 (1993)
W A Kinney et al.
Journal of medicinal chemistry, 35(25), 4720-4726 (1992-12-21)
In this report, a novel bioisostere of the alpha-amino acid, 3,4-diamino-3-cyclobutene-1,2-dione, has been incorporated into a series of compounds which are NMDA antagonists. These compounds, which are achiral and easily prepared, demonstrated good affinity at the NMDA receptor by their
Sinthuja Jegatheeswaran et al.
Vaccines, 8(3) (2020-09-23)
The carbohydrate antigen dimeric Lewis X (DimLex), which accumulates in colonic and liver adenocarcinomas, is a valuable target to develop anti-cancer therapeutics. Using the native DimLex antigen as a vaccine would elicit an autoimmune response against the Lex antigen found
O Blixt et al.
Carbohydrate research, 319(1-4), 80-91 (1999-10-16)
Reducing oligosaccharides were converted into their corresponding glycosylamines, and these were reacted with 3,4-diethoxy-3-cyclobuten-1,2-dione (squaric acid diethyl ester). The resulting derivatives could be linked to amino-functionalized lipids, solids, or proteins. Treatment of the obtained lipid or solid conjugates with aqueous

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