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Merck
CN

310778

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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线性分子式:
(C2H5O)2C4(=O)2
化学文摘社编号:
分子量:
170.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
640626
Assay:
98%
Form:
liquid
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InChI

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

SMILES string

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

InChI key

DFSFLZCLKYZYRD-UHFFFAOYSA-N

assay

98%

form

liquid

Quality Level

bp

95 °C/0.1 mmHg (lit.)

density

1.15 g/mL at 25 °C (lit.)

functional group

ether, ketone

General description

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。

Application

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。

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

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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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
The Journal of Organic Chemistry, 59, 4707-4707 (1994)
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
Organic Syntheses, 69, 220-220 (1990)

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