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Merck
CN

690198

Sigma-Aldrich

3,4-二乙氧基-3-环丁烯-1,2-二酮

≥98.0% (GC)

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
Beilstein:
640626
MDL编号:
UNSPSC代码:
12352100
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方案

≥98.0% (GC)

制造商/商品名称

Lonza Ltd

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.)

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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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

法规信息

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M G Wilkerson et al.
Journal of the American Academy of Dermatology, 13(2 Pt 1), 229-234 (1985-08-01)
Two squaric acid diesters, squaric acid diethyl ester (SADEE) and squaric acid dibutyl ester (SADBE), have been suggested as replacements for 2,4-dinitrochlorobenzene in the treatment of alopecia areata and alopecia totalis. We synthesized these squaric acid diesters and examined them
Frederik Wurm et al.
Biomacromolecules, 13(4), 1161-1171 (2012-03-02)
Polymer-protein conjugates generated from side chain functional synthetic polymers are attractive because they can be easily further modified with, for example, labeling groups or targeting ligands. The residue specific modification of proteins with side chain functional synthetic polymers using the
E F Sherertz et al.
Archives of dermatological research, 280(1), 57-60 (1988-01-01)
Squaric acid diethylester and squaric acid dibutylester have been used in contact sensitization therapy of alopecia areata. This study investigated the application of these esters or squaric acid alone to hairless mouse and human skin in vitro to determine squaric
The relationship between sensitization with squaric acid diethylester and IgE-mediated allergy.
P D Pigatto et al.
Bollettino dell'Istituto sieroterapico milanese, 63(3), 226-228 (1984-07-31)
L F Tietze et al.
Bioconjugate chemistry, 2(3), 148-153 (1991-05-01)
The coupling of p-aminophenyl 2-acetamido-2-deoxy-3-O-beta-D- galactopyranosyl-beta-D-galactopyranoside (gal-beta 1,3-galNAc) to bovine serum albumin (BSA) was achieved by using 1,2-diethoxycyclobutene-3,4-dione (squaric acid diester) as a new coupling reagent. Two selective consequential steps afforded the desired neoglycoprotein: reaction of the p-aminophenyl group of

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