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Merck
CN

689203

3,4-二羟基-3-环丁烯-1,2-二酮

Arxada quality, 98.50-101.00 % (w/w) (HPLC)

别名:

方形酸

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线性分子式:
(HO)2C4(=O)2
化学文摘社编号:
分子量:
114.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-761-4
Beilstein/REAXYS Number:
774275
MDL number:
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InChI

1S/C4H2O4/c5-1-2(6)4(8)3(1)7/h5-6H

InChI key

PWEBUXCTKOWPCW-UHFFFAOYSA-N

SMILES string

OC1=C(O)C(=O)C1=O

quality

Arxada quality

manufacturer/tradename

Arxada AG

concentration

98.50-101.00 % (w/w) (HPLC)

impurities

≤0.5 % (w/w) water (Karl Fischer)

mp

>300 °C (lit.)

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

存储类别

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

374.0 °F

flash_point_c

190 °C

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

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分析证书(COA)

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Carlos E Silva et al.
The journal of physical chemistry. A, 114(37), 10097-10109 (2010-08-26)
This work presents the crystal structure and the investigation under a supramolecular perspective of a squaric acid derivative obtained from the replacement of the hydroxyl groups by anilines. The squaraine obtained (1,2-dianilinesquaraine) crystallizes in the Pbcn space group, in a
Elena Sanna et al.
Organic letters, 12(17), 3840-3843 (2010-08-10)
A minimalist squaramide-based chemodosimeter for Cu(2+) is described. Upon selective chelation to 2, Cu(2+) induces the formation of a highly colored zwitterionic radical, which is kinetically stable for hours. The presence of a radical is confirmed by EPR and ESI-MS.
Jørn E Tungen et al.
Organic letters, 14(23), 5884-5887 (2012-11-15)
Asymmetric iodolactonization of γ- and δ-unsaturated carboxylic acids has been explored in the presence of six different chiral organocatalysts 5-8. The catalyst 6b was found to facilitate the cyclization of 5-arylhex-5-enoic acids 1 to the corresponding iodolactones 2 with up
Wen Yang et al.
Organic letters, 15(6), 1190-1193 (2013-03-08)
An efficient asymmetric cascade sulfa-Michael/Michael addition reaction catalyzed by a chiral bifunctional squaramide-tertiary amine catalyst has been developed. This organocatalytic cascade reaction provides easy access to highly functionalized chromans with three contiguous stereocenters, including one quaternary center. In addition, a
Clare E Rowland et al.
Inorganic chemistry, 49(19), 8668-8673 (2010-03-13)
Two uranyl squarates, (UO(2))(6)(C(4)O(4))(3)(OH)(6)O(2)·9H(2)O·4NH(4) (1; a = 16.6897(7) Å, cubic, I23) and (UO(2))(C(4)O(4))(OH)(2)·2NH(4) (2; a = 8.5151(4), b = 15.6822(8), c = 7.3974, orthorhombic, Pbcm), have been synthesized from ambient aqueous solutions as a function of pH. Oligomerization of the

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