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Dioxosuccinic acid, also known as oxalic acid, is a dicarboxylic acid with the chemical formula C2H2O4. It is a colorless, odorless, crystalline solid that is soluble in water and slightly soluble in ethanol. Oxalic acid is commonly found in various plants, such as rhubarb and spinach, and is also produced industrially for use in various applications, including as a cleaning agent, a bleaching agent, and a precursor in the synthesis of other chemicals. It is known for its ability to form strong complexes with metal ions, which makes it useful in removing rust and other metal stains. However, it is also toxic and can cause health issues if ingested or inhaled, so it is important to handle it with care.

7580-59-8

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7580-59-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7580-59-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,8 and 0 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7580-59:
(6*7)+(5*5)+(4*8)+(3*0)+(2*5)+(1*9)=118
118 % 10 = 8
So 7580-59-8 is a valid CAS Registry Number.
InChI:InChI=1/C4H2O6/c5-1(3(7)8)2(6)4(9)10/h(H,7,8)(H,9,10)

7580-59-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name dioxosuccinic acid

1.2 Other means of identification

Product number -
Other names Butanedioic acid,2,3-dioxo

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7580-59-8 SDS

7580-59-8Relevant academic research and scientific papers

Synthesis and spectral properties of novel fluorescent diethoxycarbonyl glycoluril derivatives

She, Nengfang,Gao, Meng,Cao, Liping,Yin, Guodong,Wu, Anxin

, p. 2533 - 2536 (2007)

A novel class of fluorescent diethoxycarbonyl glycoluril derivatives with aryl alkyne side chains was synthesized via alkylation and subsequent Sonogashira cross-coupling reactions. The fluorescence spectra showed that these compounds exhibited good blue fluorescence with the maximum wavelengths ranging from 368 nm to 403 nm. Georg Thieme Verlag Stuttgart.

Synthesis and binding properties of two new fluorescent molecular clips based on diethoxycarbonyl glycoluril

Hu, Sheng-Li,Wang, Shuai,Li, Yi-Tao,Cao, Li-Ping,Wu, An-Xin

scheme or table, p. 32 - 34 (2009/10/02)

Two new fluorescent molecular clips based on diethoxycarbonylglycoluril have been synthesised and their binding properties investigated by fluorescence spectroscopy to show that they can selectively bind Fe3+ with fluorescence quenching.

Synthesis and recognition properties of two novel concave molecules based on glycoluril

Shuai, Wang,Wu, An-Xin,She, Neng-Fang

scheme or table, p. 265 - 268 (2009/12/07)

Two new concave fluorescent molecular clips based on diethoxycarbonyl glycoluril and diphenyl acetylene units have been synthesised by introducing the fluorophores into the receptor. Their recognition properties toward various metal ions were studied by f

Synthesis of self-folded molecular rotors controlled by edge-to-face CH/π aromatic interactions

Li, Yitao,Zhu, Yanping,Qin, Jing,Guo, Huizhen,Li, Lin,Wu, Anxin

scheme or table, p. 2028 - 2034 (2009/12/31)

A series of novel self-folded molecular rotors were synthesized and characterized by 1H NMR, 13C NMR, HRMS, and IR data. All but two compounds were also studied by X-ray crystallography. Georg Thieme Verlag Stuttgart.

Sensor for nitrophenol based on a fluorescent molecular clip

She, Nengfang,Gao, Meng,Cao, Liping,Wu, Anxin,Isaacs, Lyle

scheme or table, p. 2603 - 2606 (2009/11/30)

We report the synthesis, X-ray crystal structure, and photophysics of a fluorescent molecular clip (1). Binding studies of 1 toward phenols 2a-j were carried out using fluorescence, 1H NMR, and IR spectroscopy, which revealed a high affinity and selectivity for 4-nitrophenol (2a) due to formation of the 1-2a complex driven by H-bonding and π-π stacking interactions.

A novel method of synthesis of 1,2-diketones from 1,2-diols using N-bromosuccinimide

Khurana, Jitender M.,Kandpal, Bhaskar M.

, p. 4909 - 4912 (2007/10/03)

A simple and convenient procedure is reported for the synthesis of benzils and aliphatic 1,2-diketones of cyclic and open chain compounds from corresponding hydrobenzoins and 1,2-diols by refluxing with N-bromosuccinimide in carbon tetrachloride in presence or absence of pyridine.

Oxidation of cobalt (III) bound and unbound oxalacetic acid by potassium bromate

Sankaran, K. R.,Srinivasan, Vangalur S.

, p. 277 - 279 (2007/10/02)

The title reaction exhibits total second order kinetics.To explain the formation of products, diketosuccinic acid/CoIII-diketosuccinic acid and stoichiometric results, a suitable mechanism has been proposed.

Kinetics of the Reaction of Iodine with Dihydroxyfumaric Acid

Duka, G. G.,Skutaru, Yu. V.,Sychev, A. Ya.

, p. 1190 - 1192 (2007/10/02)

The kinetics of the reaction of dihydroxyfumaric acid (DFH4) with I2 and I3- have been investigated and it has been shown that the reaction between DFH4 and I2 is very rapid (k > 2 x 107 litre mol-1 s-1), but subsequently the rate is limited by the conversion of the keto-form of the acid into the enediol form.With increase of the concentration of iodide ions, the rate of oxidation of DFH4 falls (k = 6.9 litre mol-1 s-1).The optimum conditions for the application of the reaction of I2 with DFH4 to the determination of the content of the enediol form of the acid in the dihydroxyfumaric acid-oxaloglycolic acid tautomeric mixture have been found.

Catalysis of the Oxidation of Dihydroxyfumaric Acid. Kinetics and Mechanism of the Oxidation of Dihydroxyfumaric Acid by Hydrogen Peroxide in the Presence of Iron(II) Ions

Sychev, A. Ya.,Duka, G. G.

, p. 837 - 839 (2007/10/02)

The Fe2+-dihydroxyfumaric acid (DFH4)-H2O2 system has been investigated by the kinetic grid method.The reaction is of first order with respect to Fe2+, DFH4, and H2O2, and its rate depends only slightly on the pH.The effective rate constants for reactions involving complexes with the mono- and di-anions have been estimated.It is shown that the oxidation of DFH4 by hydrogen peroxide proceeds in the same way as the oxidation by oxygen-via a cyclic mechanism.

The Kinetics and Mechanism of the Oxidation of Dihydroxyfumaric Acid by Oxygen in the Presence of Iron(II) Ions

Sychev, A. Ya.,Duka, G. G.

, p. 522 - 524 (2007/10/02)

The kinetics and mechanism of the oxidation of dihydroxyfumaric acid by oxygen, catalysed by Fe2+ ions, have been investigated by spectrophotometric and gas-volumetric methods.An expression has been obtained for the rate of oxidation and for the estimation of the effective rate constants.A cyclic mechanism is proposed.

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